NOBLE METAL NANOPARTICLES APPLICATIONS IN CANCER João Conde1,2, Gonçalo Doria1, Pedro Baptista1

1

CIGMH, Departamento de Ciências da Vida, Faculdade de Ciências e Tecnologia,

Universidade Nova de Lisboa, Campus de Caparica, 2829-516 Caparica, Portugal;
2

Instituto de Nanociencia de Aragón, Universidad de Zaragoza, Pedro Cerbuna 12,

50009, Zaragoza, Spain.

Correspondence should be addressed to Pedro Baptista, pmvb@fct.unl.pt

ABSTRACT

Nanotechnology has prompted new and improved materials for biomedical applications with particular emphasis in therapy and diagnostics. Special interest has been directed at providing enhanced molecular therapeutics for cancer where conventional approaches do not effectively differentiate between cancerous and normal cells, i.e. lack specificity. This normally causes systemic toxicity and severe and adverse side effects with concomitant loss of quality of life. Because of their small size, nanoparticles can readily interact with biomolecules both at surface and inside cells, yielding better signals and target specificity for diagnostics and therapeutics. This way, a variety of nanoparticles with the possibility of diversified modification with biomolecules have been investigated for biomedical applications including their use in highly sensitive imaging assays, thermal ablation and radiotherapy enhancement, as well as drug and gene delivery and silencing. Here, we review the available noble metal nanoparticles for cancer therapy, with particular focus on those already being translated into clinical settings.

KEYWORDS: Noble metal nanoparticles; Gold nanoparticles; Silver nanoparticles; Cancer; Oncology; Therapeutics; Theranostics; Imaging

INTRODUCTION

Cancer is one of the leading causes of mortality in the modern world, with more than 10 million new cases every year [1]. It is well established that cancer is a multifactorial disease caused by a complex mixture of genetic and environmental factors [2-4], where considerable advances have led to a more comprehensive understanding of cancer at the genetic, molecular, and cellular levels providing new targets and strategies for therapy [5]. Nevertheless, these advances have yet to be effectively translated into functioning diagnostics and therapy. For example, the effectiveness of many anticancer drugs is limited due to the inability to reach the target site in sufficient concentrations and efficiently exert the pharmacological effect without causing irreversible unwanted injury to healthy tissues and cells [6,7]. The technological leap of controlling materials at nanoscale provides for a “big revolution” in medical and healthcare treatments and therapies [8,9]. Nanotechnology offers a wealth of tools to diagnose and treat cancer - new imaging agents; multifunctional, targeted devices capable of bypassing biological barriers to deliver therapeutic agents directly to cells and tissues involved in cancer growth and metastasis; monitor predictive molecular changes allowing preventive action against precancerous cells; minimizing costs and side effects [5,10,11]. Nanotechnology based therapies for cancer with minimal side effects and high specificity are on the surge, where the main challenge is to develop a system for molecular therapy capable of circulating in the blood stream undetected by the immune system and recognize the desirable target, signaling it for effective drug delivery or gene silencing with minimum collateral cell damage - nanovectorization. As a result, personalized medicine could become a reality in cancer patient management.

Nanoparticles (NPs), and noble metal NPs in particular, are versatile agents with a variety of biomedical applications including their use in highly sensitive diagnostic assays [12,13], thermal ablation and radiotherapy enhancement [14-17], as well as drug and gene delivery [18-21]. Moreover, noble metal NPs have been proposed as non-toxic carriers for drug and gene delivery applications [22-24]. Additionally, the nanoparticlebased systems can provide simultaneous diagnostic and therapy, i.e. Theranostics, exploring their unique properties for better penetration of therapeutic moieties and

tracking within the body, allowing a more efficient therapy with a reduced risk in comparison to conventional therapies [25] – see Figure 1.

Figure 1. Noble metal NPs for cancer therapy. Once the tumor is directly connected to the main blood circulation system, NPs can exploit several characteristics of the newly formed vasculature and efficiently target tumors. Tumor cells are supplied by blood capillaries that perfuse the cells of the tissue where NPs can i) passively accumulate or ii) anchor through targeting moieties to biomarkers overexpress by tumor cells. NPs can act simultaneously as therapeutic agents, inducing hyperthermia, enhancing radiotherapy, silencing genes and/or delivering drugs to induce tumor cell death; and as imaging enhancers or contrast agents, to help tracking the therapeutic effects in real time.

The unique characteristics of noble metal NPs, such as high surface-to-volume ratio, broad optical properties, ease of synthesis and facile surface chemistry and functionalization hold pledge in the clinical field for cancer therapeutics [22,26,27]. Noble metal NPs (e.g. gold, silver or a combination of both) present highly tunable optical properties, which can be easily tuned to desirable wavelengths according to their shape (e.g. nanoparticles, nanoshells, nanorods, etc.), size (e.g. 1 to 100 nm) and composition (e.g. core/shell or alloy noble metals), enabling their imaging and

thus enabling thermal ablation of targeted cancer cells [31.photothermal applications under native tissue [28. nanotechnology based systems could offer a less invasive alternative. the results of which are judged to be desirable and beneficial [33]. such as antibodies. enhancing the life expectancy and quality of life of the patient [35]. Making use of their extraordinary properties. we will focus on the application of noble metal NPs for cancer therapy with particular emphasis on their use in vivo and their potential to be translated into clinical settings.37]. universally targeting cells within a tumor is not always feasible because some drugs cannot diffuse efficiently and the random nature of the approach makes it difficult to control the process and may induce multiple-drug resistance  a situation where chemotherapy treatments fail due to resistance of cancer cells towards one or more drugs [7]. polyethylene glycol.32].29]. Among these. In this review. they can efficiently convert light or radiofrequencies into heat. peptides and/or DNA/RNA to specifically target different cells [30]. THERAPY In medical terms a therapeutic effect is a consequence of a medical treatment of any kind. These NPs can also be easily functionalized with various moieties. and with biocompatible polymers (e. 1. Efficient in vivo targeting to heterogeneous population of cancer cells and tissue still requires better selectivity and non-cytotoxicity to surrounding healthy cells. PEG) to prolong their in vivo circulation for drug and gene delivery applications [23.g. Moreover.24]. Conventional therapy methods in cancer involve the employment of agents that do not greatly differentiate between cancerous and normal cells. . leading to systemic toxicity and adverse and severe side effects [34]. the potential therapeutic application of noble metal NPs represents an attractive platform for cancer therapy in a wide variety of targets and clinical settings [36. However.

49] and RNA interference (RNAi) via use of small-interfering RNA [50-53] have emerged as a powerful and useful tools to block gene function and for . such as PEG. thus. Gene Silencing Antisense DNA [48. peptides and/or DNA/RNA to specifically target extracellular and intracellular receptors or pathways [30]. can also greatly increase their solubility. such as antibodies. DNA and RNA macromolecules can be used to simultaneously target specific sequences and exert their genetic-based therapy [42. leading to more efficient control of their therapeutic properties.2.1. help evading macrophage-mediated uptake and.39-41]. NPs targeting strategies to cancerous tissues have focused on passive and active targeting. functionalization of the NP’s surface with hydrophilic molecules.8. demonstrating targeting by enhanced permeation and retention. For active targeting. capable of simultaneously target and deliver multiple therapeutic agents. leading to tumor cell death with minimal damage to collateral healthy cells [36. such as monoclonal antibodies.e. In nucleic-acid functionalized NPs. i. The use of NPs functionalized with multiple peptides or antibodies. because numerous tumors present defective vasculature and poor lymphatic drainage due to the rapid growth of solid tumors.43].45] or fluorescent [46. In passive targeting. thus accumulation at the tumor site [6. they can also be functionalized with chemical moieties. NPs can be easily functionalized with a wide variety of biological moieties.38]. such as Raman [44. have been described to successfully target specific cell surface proteins or receptors on cancer cells and further direct their antitumor action. 1. Tumor targeting It is expected that the greatest gains in therapeutic selectivity will be achieved by synergistic combinations of several multicomponent targeting strategies. noble metal NPs can extravasate into the tumor stroma through the fenestrations of the angiogenic vasculature. Additionally. while avoiding the organism’s biological and biophysiscal barriers.47] reporters.1. To help tracking noble metal NPs in vivo and enhance the imaging properties of such moieties. avoid removal from the systemic circulation and protect their carriers from enzymatic degradation when used in vivo [30].

43]. For example. one drawback of using naked siRNAs is that they show extremely short half-lives. They have also shown that polyvalent RNA-AuNP conjugates are readily taken up by cells. as nanoscale devices. can readily interact with biomolecules on both the surface of cells and inside of cells for longer periods of time [10]. Gold NPs (AuNPs) have shown potential as intracellular delivery vehicles for antisense oligonucleotides [55] and for therapeutic siRNA by providing protection against RNAses and ease of functionalization for selective targeting [42. weak protection against action by RNases.58-60]. AuNPs modified with the hydrophilic PEG polymer. Several other studies using engineered NPs modified with siRNA have demonstrated a cytoplasmic delivery system of siRNA and efficient gene silencing using AuNPs [42. . the major obstacle to clinical application is the uncertainty about how to deliver miRNAs with maximal therapeutic impact. providing a highly efficient gene regulator in terms of high loading of the antisense DNA with no toxicity at the concentrations studied [55]. and that the particle bound siRNA could effectively regulate genes in the context of RNA interference [42]. Mirkin and coworkers showed that AuNPs attached to single stranded oligodeoxynucleotides can be used for gene therapy. Also. poor chemical stability and common dissociation from vector [54]. In fact. which in turn is affected by the amount of siRNA that is delivered and on the potential of each siRNA to suppress its target. developed an Au-nanoshell functionalized with TAT-lipid layer for transfection and selective release of siRNA [57]. playing an important role in down-regulation of specific gene expression in cancer cells. Nanotechnology offers an unprecedented opportunity to overcome these problems. siRNAs and then coated with poly(β-aminoester)s have been shown to facilitate high levels of in vitro siRNA delivery and gene silencing in human cells [56]. The authors demonstrated that this NIR strategy for siRNA release was proficient and timedependent. Thus. due to their small size. Braun et al.sequence-specific post-transcriptional gene-silencing.56. Small-interfering RNAs (siRNAs) can be transfected into mammalian cells by a variety of methods that influence the strength and duration of the silencing response. where the TATlipid coating was used to efficiently mediate the cellular uptake of the nanoconjugates and the siRNA release was dependent on near-infrared (NIR) laser pulses.

In fact.76] and . It combines two key components: i) light source. which are lower than normal healthy tissue due to their poor blood supply. killing them selectively. magnetic NPs have been introduced in the body through magnetic delivery systems or local injection to the affected area [63].3. and it is commonly accepted that above 42 °C cell viability is strongly reduced. The first in vivo Phase II clinical trials of magnetic NP hyperthermia were undertaken in Germany in 2005 [64] by injecting the prostate of cancer patients with biocompatible magnetite NPs.69]. El-Sayed and coworkers demonstrated that Au-nanorods are effective photothermal agents due to their longitudinal absorption band in the NIR on account of their SPR oscillations [65. In nanoparticle mediated hyperthermia for cancer. This can be achieved by exposing the entire patient or the targeted area to an alternating current magnetic field. an intense light source or radiofrequencies which will cause the NPs to heat up and induce thermal ablation of the tumor. such as lasers with a spectral range of 650–900 nm [66] for deep tissue penetration. hyperthermia effects can range from moderate denaturation of blood and extracellular proteins to induction of apoptosis and. Since NIR light transmits readily through human skin and tissue.Hyperthermia Hyperthermia is based on the effect increasing temperatures have on living cells. these nanorods can be used as ablation components for cancer [70.1. One of the most widespread examples of hyperthermia mediated by NPs. Noble metal NPs have thoroughly been used as photothermal agents for in vivo therapy as a less invasive experimental technique that holds great promise for the treatment of cancer [65]. Au-nanocages [67. For example. NPs heat up cancerous cells beyond their temperature tolerance limits. Other gold nanostructures such as Au-nanoshells [72-74]. Small diameter Au-nanorods are being used as photothermal converters of near infrared radiation (NIR) for in vivo applications due to their high absorption cross sections beyond the tissue absorption spectra. Hyperthermia therapy in cancer has been widely used either via direct irradiation or suitable temperature vectors. to cell death and tissue ablation [61]. and ii) optical absorbing NPs which efficiently transforms the optical irradiation into heat on a picosecond time scale.71].75.68]. above 50 °C. Successful results were obtained using minimally invasive ablation of the tumor in an AC magnetic field after several sessions. such as metal NPs [62]. thus inducing photothermal ablation [67.66.

exceeding the . The rapid heating of Aunanoshells upon NIR laser irradiation allowed for effective photothermal ablation of tumor in the mouse [78]. After intravenous injection. completely inhibiting the tumor growth after just five days of treatment [80]. In vivo rat exposures to 35 Watts using direct AuNPs injections resulted in significant thermal injury at subcutaneous injection sites.56 MHz have also been shown to induce heat in AuNPs and thermally destroy tumor tissue [84]. described the use of AuNPs for skin tumor therapy based on local laser-inducing hyperthermia. The photothermal properties of AuNPs can also be used to generate transient vapor nanobubbles in order to produce a tunable nanoscale theranostic agent. due to the evaporation of a very thin volume of the surrounding medium. Radiowaves have the advantage of presenting significantly better penetration on tissue than NIR light. Plasmonic nanobubbles have been successfully applied as an in vivo tunable theranostic cellular agent in zebrafish hosting prostate cancer xenografts and in leukemia cells of human bone marrow specimens. making them more efficient for deeper solid tumors [85]. The use of noninvasive radiowaves at 13.spherical AuNPs [77] have also demonstrated effective photothermal destruction of cancer cells and tissue. Gold-silver (AuAg)-nanorods labeled with molecular aptamers proved to require up to six orders of lower laser power irradiation to induce cell death when compared to Aunanoshells or Au-nanorods [86]. the AuNPs accumulated in the skin tumor cells after 4-5 hours and induced apoptotic death of tumor cells.83]. described as plasmonic nanobubbles [81]. These aptamer Scg8-AuAg-nanorods conjugates presented excellent hyperthermia efficiency and selectivity to CEM cells. PEG-modified Au-nanoshells (Silica/Au core/shell NPs) injected intravenously in tumor-bearing mice showed to passively accumulate in the tumor tissue due to the leakiness of the tumor vasculature. thus enhancing the photothermal effect in cancer cells [79]. A similar approach was used by Terentyuk et al. These nanobubbles are generated when the AuNPs are locally overheated with short laser pulses. which in turn creates a vapor nanobubble that expands and collapses within nanoseconds. Sirotkina et al. despite their greater depth of penetration there is also greater energy attenuation by tissue. where plasmonic silica/gold nanoshells were used to produce a controllable laser hyperthermia in tissues. Nonetheless.. presenting higher therapeutic selectivity when compared with AuNPs alone [82.

As a consequence. Cheng and coworkers evaluated the photothermal efficiencies of three Au-based nanomaterials (silica@Au-nanoshells. Likewise. distribution into healthy tissues leads to severe side effects. These systems show evidence of enhanced delivery of unstable drugs. Drug delivery The vast majority of clinically used drugs for cancer are low molecular-weight compounds that diffuse rapidly into healthy tissues being evenly distributed within the body. drug release rate and particle disintegration. described the first example of 2 nm AuNPs covalently functionalized with the chemotherapeutic drug paclitaxel [92]. oxaliplatin.4. 1.g. whereas hollow Au/Ag nanospheres and Au-nanorods needed increasingly higher concentrations. such as paclitaxel [92] or Platinum(Pt)-based drugs (e. The NPs’ performance as drug vectors depends on the size and surface functionalities of the particles. AuNPs have already been used as vehicles for the delivery of anticancer drugs. increase cancer cell death [89. more targeted distribution and capability to evade/bypass biological barriers. HeLa cervix cancer cells and TCC bladder cancer cells) using a CW NIR laser [88]. thus. hollow Au/Ag nanospheres and Au-nanorods) at killing three types of malignant cells (A549 lung cancer cells. The administrations of hydrophobic drugs require molecular encapsulation and it is found that nanosized particles are particularly . Bimetallic AuAg-nanostructures with a dendrite morphology and hollow interior have also been developed as photothermal absorbers to destroy A549 lung cancer cells [87]. such as multi-drug resistance [91].affinity of the original aptamer probes alone. relatively small amounts of the drug reach the target site and. nanoparticles can be used as vectors for targeting cancer tissue/cells so as to optimize biodistribution of drugs. As seen above. The photothermal performance of such dendrites required lower NP concentrations and laser power for efficient cancer cell damage when compared to Au-nanorods photothermal therapeutic agents. Silica@Au-nanoshells needed the lowest NP concentration for effective photo-ablation. exhibit a short half-life in the blood stream and a high overall clearance rate. cisplatin.90]. Poor drug delivery and residence at the target site leads to significant complications.94]. etc. Gibson et al. Gold has also been used together with magnetic or paramagnetic materials to enhance the photothermal effect and.) [93.

Radiotherapy Radiotherapy uses ionizing radiation for cancer treatment to control the proliferation of malignant cells. with smaller size particles (20 and 50 nm) being the most cytotoxic at relatively harmless radiation doses. The irradiation may also be used to activate the NPs and set up the release of their cytotoxic action. AuNPs. 20 and 40 nm AuNPs and 20. upon X-ray irradiation. Hypothetically. the different coatings of the AuNPs used may be responsible for the different outcomes observed. 1. The use of this strategy has led to improvement in the treatment on cancer cells with little or no increase in harm to normal surrounding tissues in mice models [15] and also in breast cancer [98]. the delivery of a lethal dose of radiation to a tumor while sparing nearby healthy tissues remains the greatest challenge in radiation therapy. Treating glioma cells with AgNPs led to radiation dose-dependent cytotoxicity. These nanoshell-composite hydrogels where designed to strongly absorb NIR light and release multiple bursts of any soluble material held within the hydrogel matrix in response to repeated NIR irradiation. Nonetheless. . Xia and coworkers developed a similar approach using 50-nm hollow Aunanocubes (nanocages) with eight lopped-off porous corners covered by a thermosensitive polymer containing a pre-loaded effector that can be later released in a controllable fashion using a NIR laser [18]. which contrasted with the results of previous studies performed with AuNPs coated with PEG or amino acids in mice colorectal adenocarcinoma and breast cancer cells [15. all modified with proteins from fetal bovine serum [99]. providing enhanced radiation targeting with lower radiation doses. consequently avoiding damage to healthy tissues.98].efficient in evading the reticuloendothelial system [95]. More recently. can act as dose enhancers and/or generate radicals that damage cancer cells and induce cell apoptosis. AuNPs showed little effect on cell survival across different doses of ionizing radiation. Gold–gold sulfide nanoshells covered by a thermosensitive hydrogel matrix have been developed as a photothermal modulated drug delivery system [96]. and have been proposed as potential radiosensitizers for X-ray cancer therapy [97]. Noble metal NPs can act as antennas. 50 and 100 nm silver nanoparticles (AgNPs).5. In this study. Gu and coworkers studied the potential effects on radiation-induced killing of glioma cells mediated by 10. More recently.

The use of platinum NPs (PtNPs) as prominent radiation sensitizers in radiotherapy cancer treatment showed strong enhancement of the biological efficiency of radiations. nanoshells. leading to amplified lethal damage in DNA from tumor cells. . 2.110]. However. most noble metal NPs can be used for the simultaneous actuation and tracking in vivo – see Figure 2. or as contrast agents for Computed Tomography (CT) [103]. most noble metal nanomaterials are capable of combining multiple imaging modalities that can yield complementary information and offer synergistic advantages over any single imaging technique [109. Magnetic Resonance Imaging (MRI) [104]. such as NPs. Because light absorption from biologic tissue components is minimized at near infra-red (NIR) wavelengths. IMAGING Along with their therapeutic capabilities. nanocages and nanorods. Optical Coherence Tomography (OCT) [105-107] and Photoacoustic Imaging (PAI) [108]. most noble metal NPs for in vivo imaging and therapy have been designed to strongly absorb in the NIR so as to be used as effective contrast agents [100]. have showed widespread application as contrast agents for in vivo cancer imaging: those presenting a significant absorbance and scattering in the NIR region [46. Moreover.101] or Surface-enhanced Raman scattering (SERS) [102]. noble metal nanomaterials. when compared to metal atoms [37]. nanoclusters.

These innovative NPs comprise nucleic acids. polymers and antibodies that can used to improve NP circulation. Multifunctional systems can carry reporter molecules tethered to the particle surface and employed as tracking and/or contrast agents. Hybrid NPs with a super-paramagnetic iron oxide/silica core and a gold nanoshell. allow to overcome the limitations of conventional contrast agents (e. aptamers and anticancer drug molecules for delivery to the target tissue.g. delivery and imaging. which could lead to increased risk to public health [111]. iodine-based compounds). which allows to reduce the radiation dosage needed. Typically. have been used . with significant absorbance and scattering in the NIR region. renal toxicity and vascular permeation [103].Figure 2. Three-dimensional imaging can be achieved by Computed Tomography (CT). they can be on the surface or inside the NPs. Depending on the targeting mechanism. The use of ~30 nm PEG-coated AuNPs for in vivo CT contrast agent was shown to increase image contrast. peptides. Responsive NPs/molecules can also trigger reaction upon external stimuli through the functionality of valuable tumor markers. effectiveness and selectivity. the cross-sectional images are acquired using X-ray radiation involving larger radiation doses than the conventional X-ray imaging procedures. where a series of plane-cross-sectional images along an axis are interlinked by computer to create a 3D image. Multifunctional NP-based systems for tumor targeting. such as short imaging times due to rapid renal clearance.

. The extra scattering achieved by using Au-nanoshells has been shown to provide an enhanced optical contrast and brightness for improved diagnostic imaging of tumors in mice due to the preferential accumulation of the nanoshells in the tumor. the image contrast enhancement effect could be isolated by continuously scanning the sample with a lower scan frequency. Optical Coherence Tomography (OCT) is an imaging modality that provides crosssectional subsurface imaging of biological tissue with micrometer scale resolution. specially due to their more compact size (<50 nm compared to >100 nm for Au-nanoshells) and larger optical absorption cross sections when compared to Au-nanoshells. Wang and coworkers have used this technique to image the distribution of Au-nanoshells circulating in the vasculature of a rat brain by achieving a gradual enhancement of the NIR optical absorption in the brain vessels [115]. Wang et al. Similarly.in vivo as dual contrast agents for CT and Magnetic Resonance Imaging (MRI) presenting high CT attenuation and a good MR signal in hepatoma. proposed a noninvasive in vivo spectroscopic photoacoustic sentinel lymph node mapping using gold nanorods as lymph node tracers in a rat model [117]. Additionally. Photoacoustic Imaging (PAI) and Photoacoustic Tomography (PAT) are noninvasive imaging techniques capable of resolving the optical absorption map of tissue at penetration depths akin with ultrasound imaging. these nanocages were shown to be better suited for in vivo applications. Moreover. Tseng et al. allowing to effectively control the therapeutic modality. allowing a more detailed image of vascular structures at greater depths. developed nanorings with a localized surface plasmon resonance covering a spectral range of 1300 nm that produced both photothermal and image contrast enhancement effects in OCT when delivered into pig adipose samples [113]. compensating for the weakness of each modality [112]. Gold-nanorods show the maximum of the plasmon resonance tuned further into the NIR that allowed Motamedi et al. These Au-nanocages enhanced the contrast between blood and the surrounding tissues by up to 81%. [78]. to develop a contrast agent for a laser optoacoustic imaging system for in vivo detection of gold nanorods and to enhance the diagnostic power of optoacoustic imaging [116]. gold capped nanoroses have been used in photothermal OCT to detect macrophages in ex vivo rabbit arteries [114].

multiplex capabilities.120].Also.or AgNPs with an attached reporter species with a Raman signature can be explored to highlight cellular structures and provide molecular structural information on the cellular environment in live cells [119. TOXICITY Both in vivo and in vitro. low quantum yield and detection sensitivity. The use of such NPs allows for higher spectral specificity. Surface-enhanced Raman scattering (SERS) using Au. improved contrast and photostability to Raman-based imaging techniques. These Au-nanoshells were also used by Bickford et al. noble metal NP probes can be used for in situ diagnostics of cancer. demonstrated the use of NIR scattering Au-nanoshells as a contrast agent in darkfield microscopy to target anti-human epidermal growth factor receptor 2 (HER2). Loo et al. such as dark-field or dual-photon luminescence microscopy. nanoparticles have a tendency to accumulate within various types of cells with special affinity for macrophage-type cells (both histiocytes and blood phagocytic cells) and reticuloendothelial cells throughout the body. insufficient stability in biological systems and weak multiplexing capability. NP-based NIR probes can overcome several limitations of conventional NIR organic dyes. bone marrow. the high scattering properties of these NPs can enhance contrast of imaging systems based on microscopy. such as poor hydrophilicity and photostability. In situ monitoring of photothermal nanotherapy of LNCaP human prostate cancer cells by SERS has been observed where a significant enhancement of the Raman signal intensity by several orders of magnitude [44]. as well as to achieve longer lifetime emission signals that overcome cellular autofluorescence interference. They also produce varying degrees of bioaccumulation in such tissues as lymph nodes. Additionally. . 3. for imaging live HER2-overexpressing cancer cells using two-photon microscopy [118]. The silver shell allowed to enhance emission intensity up to 6-fold and photostability by 2-fold. These metal nanoshells were composed of silica spheres with encapsulated Ru(bpy) 32+ complexes as core and thin silver layers as shell. developed fluorescent metal nanoshells as molecular imaging agents to detect single microRNA (miRNA) molecules in lung cancer cells [47]. Zhang et al. For example. a clinically significant breast cancer molecular marker [72].

These results seemed to confirm size dependent toxicity of AuNPs. Silver NPs are generally considered more toxic than AuNPs. an inference that has hitherto been shown to be somewhat ambivalent [129-134]. adrenals. followed by cube-shaped AuNPs. dramatically led to a decrease in the population of the macrophages and up-regulated the expressions of proinflammatory genes interlukin-1. while sphere-shaped AuNPs displayed the best biocompatibility. studied the in vivo toxicity of AuNPs according to their shape in KM mice showing that rod-shaped AuNPs were the most toxic.spleen. AuNPs are considered to be benign but the size similarity to biological molecules could provide “camouflage” to cellular barriers. Sun et al. The NPs size plays an important role in avoiding immune activation and renal clearance. Moreover. this study revealed that all AuNPs accumulated preferentially in the liver and spleen organs [136]. whereas. liver and kidneys [121-123]. with several studies showing that cell exposure to AgNPs induced significant cytotoxicity [138-141]. which may explain their toxicity in the previous studies [137]. In fact. noble metal NPs have been shown to induce DNA damage and oxidative damage [124-126]. hydrophilic NPs ranging in size between 10 and 100 nm are small enough to slow down activation of the mononuclear phagocyte system but are big enough to avoid renal filtration [8]. interlukin-6. Yen et al. showed that AuNPs. especially those of smaller sizes. In fact. Research shows that NPs can stimulate and/or suppress the immune responses. Generally. A systematic investigation of the size-dependent cytotoxicity of AuNPs against four cell lines found that 1 to 2 nm AuNPs displayed cell-type dependent cytotoxicity with high micromolar IC50s. and that their compatibility with the immune system is largely determined by their surface chemistry. is well known the influence of size. revealing that toxicity is shape-dependent. . For example. and tumor necrosis factor alpha [135]. solubility and surface modification on the biocompatibility of NPs and their use in biological applications [122]. 15 nm AuNPs were nontoxic to cells at concentrations 60-fold higher than the IC50 of the smaller AuNPs [128]. Nonetheless. leading to undesired cellular entry which might be detrimental to normal cellular function [127]. thus enhancing their circulating time and availability for effective therapy. In terms of acute toxic effects to cells. it is worth pointing out that CTAB (a cationic surfactant commonly used for Au-nanorods synthesis) was also recently pointed out as the source of Au-nanorods’ cytotoxicity.

Asharani et al. As for platinum. CONCLUSIONS Nanotechnology has provided for novel and powerful systems that may be used treatment and diagnostic of cancer.) constitutes another interface of interaction with the organism’s proteins and cells. which can explain the discrepancy with other studies related to AgNPs cytotoxicity [135]. thus contributing to the overall effects of the use of the nanoparticles. In fact. In vivo demonstrations of noble metal NPs as theranostic agents are now emerging and serve as important milestones towards clinical application. shape. concluding that AgNPs were the most toxic. leading to an increase in DNA damage. and administration pathways. such as surface chemistry. determined a lower cytotoxicity of AgNPs than that of the AuNPs and attributed this difference to the surface charges between NPs. such as pharmacokinetics. where PtNPs were shown to enter the cells through diffusion.g. followed by PtNPs. Even though we have focused our attention on the toxicity aspects of the different noble metal nanoparticles based mainly on size and metal. reagents and drugs being used for the development of these nanoscale theranostic agents have still to be approved by the main supervising agencies.and 15-35 nm AuNPs capped with PVA in developing zebrafish embryos.Conversely. the cytotoxicity of 5-8 nm PtNPs capped with polyvinyl alcohol (PVA) has been addressed in human cells. the majority of products. which in term may be associated with unspecific adsorption or specific recognition by the immune system. while AuNPs presented no indication of toxicity [142]. Nonetheless. Thus far. there are some questions whose answers still provide no clear understanding about the design and application of NPs. such as the FDA and EMA. performed a comparison between toxicity of 3-10 nm Pt-. surface chemistry (e. 5-35 nm Ag. The interaction with the immune system contributes not only for the specificity of the targeting (passive and/or active) but also towards the toxicological effect of nanoconjugates [see reference 122 and references therein]. Yen et al. etc. stabilizers. attention should also be brought upon other properties of the nanoconjugates. . proliferating cell nuclear antigenmediated growth arrest and apoptosis [126]. biodistribution and side effects of the nanotherapy. functionalization with biomolecules.

Are noble metal NPs cytotoxic or biocompatible? And how can the NPs be design to avoid these effects? These seem to question more difficult to answer than previously believed. roughness or interruptions could lead to complement or antibody attachment. there are important findings that can be applied for increasing nanoparticle biocompatibility and reducing cytotoxic interactions in vivo and in vitro. using the lowest NP dose to get the desired response for the shortest period of time seems to promote biocompatibility. It is essential to test nanoparticle/biological interactions experimentally and modify the NPs for best biocompatibility with the cell in order to eliminate damage to healthy tissue. decreasing bioavailabilty at target cell [143]. .safety profile of NPs before and after conjugation and toxicity [10]. In general. the presence of cracks. Most therapeutic and imaging approaches based on noble metal NPs rely on AuNPs. Even though there is not any general mechanism for making NPs universally ‘non-toxic’ to all living cells and all organisms. such as cancer itself. When interpreting NPs interactions with biological cells and organisms. it is important to remember that living systems may appear normal and be capable of growth and function. a more comprehensive application of core/shell or alloy noble metal NPs. that may allow combination of the benefits of each noble metal into a single carrier. guarding against alterations in genetic/molecular function while killing the abnormal cells. Noble metal nanoparticles have shown to be powerful tools against cancer. since a non-continuous covering. which can produce serious consequences at some time in the distant future. though still in need of further optimization and characterization for full understanding of their whole potential. but they may be genetically altered in subtle ways following NP exposure. or dissolution of the coating by cell digestion. is still to be thoroughly addressed. Nonetheless. It is now time to start translating these promising platforms to the clinical settings towards widespread effective therapy strategies in the fight against cancer. The coating/capping of a nanoparticle is also of the utmost relevance. mostly due to their higher level of non-toxicity.

T. Doria. 4. P. no.” Trends in Biotechnology. “The hallmarks of cancer. no. K. A. Langer. 2009. M. Tan. Davis. “Gold nanoparticles for the development of clinical diagnosis 1. vol. “Nanocarriers as an emerging platform for cancer therapy.Genetics. Pereira. Peer. Ferrari. pp. 2007. 2008.” Cell. 161-171. 3. 411. 80-88. vol. “Cancer Nanotechnology . vol. 26. 6. R. 2. P.” Current Cancer Therapy Reviews. “Cancer nanotechnology: opportunities and challenges. J. A. “The genetics and genomics of cancer. P. Quaresma and R. Ponder. J. 2007. 2001. Mandal. 59. P. 2005. 11. “Composite nanoparticles take aim at cancer. Balmain. pp. 33 Suppl. vol.” Nature Reviews Cancer. 1. J.” Nature. G. I. 251-265. “Cancer genetics. “Cancer Statistics. C. no. A. vol. R. 2003. Praetorius and T. pp. 1. K. vol. 2. 57-70. 11. Hanahan and R. 26. Baptista. D. no. Baptista. 2. S. Parak. O. Karp. Hong. Miranda. Jemal. pp. “Engineered nanoparticles in cancer therapy. 2010. 2000. Margalit and R. P. D. 2010. 7. 12. pp.” ACS Nano. vol.” Nature. no.” Annual Review of Medicine. Gil and W. pp. 5. E. 238-244. Selvan. pp.” CA: A Cancer Journal for Clinicians. “Nanotechnology and cancer. R. R. pp. 60. 2008. Ward. 2008. Gomes. 10. Franco. 1. pp. “Functional and multifunctional nanoparticles for bioimaging and biosensing. no. Siegel. Weinberg. Farokhzad. J. 100. 11631-11641. 8. no. 9. no. . vol. 277-300. Gray and B. Sanvicens and M. 2010. 14. vol. 8. pp. Ponder. M. 3. Heath and M. S. T. 2200-2205. B. vol. vol. 6835. 37-51. 5.” Nature Nanotechnology.REFERENCES A. pp. E. Jana. 13. 5. N.Prospects for Cancer Diagnostics and Therapy. R. “Multifunctional nanoparticles--properties and prospects for their use in human medicine. no. D. T. vol.” Langmuir. Eaton. N. pp. Xu and E. 2. Yi and N. J. 12. 336-341. Marco. P. A.” Recent patents on drug delivery & formulation. 751-760. P. 425-433.

Hainfeld. 681-693. M. Young and C. P. E. Slatkin and H. N. Schwartz. Y.” Proceedings of the National Academy of Sciences U. K. 2007. Xie. H. Wang and Y. D. vol. C. Mirkin. X. J. “Gold nanocages covered by smart polymers for controlled release with near-infrared light. R. Huang. Smilowitz. M. Cheng.” Physics in Medicine and Biology. 1461-1465. Zhang. 935-939. 14. Dilmanian. no. Yavuz. “Nanoshell-mediated near-infrared thermal therapy of tumors under magnetic resonance guidance. J. “Conjugation to gold nanoparticles enhances polyethylenimine's transfer of plasmid DNA into mammalian cells. N309–315. 2009. B. 20. vol. “Plasmonically controlled nucleic acid dehybridization with gold nanoprisms. no. “Multi-functional gold nanoparticles for drug delivery. A. 8. Rotello. Q. F. 2003. V. D. 3. pp. J. Chemphyschem.” Advances in Experimental Medicine and Biology. no. 9-10. R. Millstone. Ghosh and V. vol. vol. “Radiotherapy enhancement with gold nanoparticles. J. 977-985. G. K. 2008. I. Stafford. 2007. 100. R. F. vol. Halas and J. El-Sayed. S.” Proceedings of the National Academy of Sciences U. pp. L. K. pp. Hazle. Jain. N. M. 9138-9143. 19. Hirsch. no. pp. G. . 13549-13554. Cobley. 49. 5.” Nature Materials. no. 18. 60. 100. A. Klibanov.S. Smilowitz. R. J. J. Sershen. Xia. Giljohann. M.methods. F. 2003. pp. 391.A. 16. D. Seferos. 10.S. M. R. El-Sayed and M. L. Slatkin and H. Thomas and A. 8. 21. 2. 23. C. J. A. vol. S. H. Hainfeld. “Gold nanoparticles: interesting optical properties and recent applications in cancer diagnostics and therapy. 943-950. M. D. A. M. M.A. 15. Rivera. no. 2008. “The use of gold nanoparticles to enhance radiotherapy in mice. M. J. pp. Chen. vol. 4856. pp. N. S. 2004. Bankson. A. A. L. E. 2009. no. Kim. 18. P.” Nanomedicine (Lond). no. 620. pp. Song. pp. J. L. D. 16. 12. West. vol. vol. Price. Jones. Rycenga.” Journal of Pharmacy and Pharmacology. 17. Han.” Analytical and Bioanalytical Chemistry.

” Small. H. pp. pp. 62. S. Sau. “Gold nanoparticles in delivery applications.” The Journal of Physical Chemistry. F.” Advanced Materials.” Advanced Drug Delivery Reviews. C. 2008. “Understanding the photothermal conversion efficiency of gold nanocrystals. Parak. “Properties and applications of colloidal nonspherical noble metal nanoparticles. 6. Parak. . Kim and V. 1805-1825. 23. K. M. M. I. J. and Engineering Sciences. Mathematical. F. 29. 1333-1383. vol. Zhao. Han. shape. J. pp. and metal composition. Rivera.” Pharmaceutical Research. Sperling and W. Zanella and W. Klar and J. K. 60. no. 2011. X. 237-259. A. 2. A. Lee and X. pp. 1915. R. Feldmann. Sperling. 11. 1064-1079. vol. no. 2007. S. G. 26. pp. 16. 2. “Biological applications of gold nanoparticles. Z. 1896-1908. K. Sun. 39. no. 11. Jain. K. 41. N. pp. 110. 2010. C. P. 2010. 27. T. El-Sayed and M. A. Physical. no. vol. 2010. L. pp. T. 2272-2280. Xie. no. no. Nishiyama. Ghosh. S. Shao. L. 25. 2006.” Chemical Society Reviews. 30. pp. Yang and J. pp. 20. 9. 2010. B. no. Huang. Mukherjee. A. H. Chen. and medicine. vol. 28.” Advanced Drug Delivery Reviews. Wang. vol. 1578-1586. vol. Ming. 37. T. Chen. vol. “Nanomedicine: nanocarriers shape up for long life. 28.” Philosophical Transactions. pp. B. Gil P. 2008. no. biology. vol. sensing. “Inorganic nanoparticles in cancer therapy. R. A. R. 12. vol. Rogach. no. El-Sayed. 2008. Series A. “Noble metals on the nanoscale: optical and photothermal properties and some applications in imaging. vol. Rotello. Zhang. functionalization and bioconjugation of colloidal inorganic nanoparticles.” Nature Nanotechnology. Kudgus. M. 368. El-Sayed. no. R.” Accounts of Chemical Research. “Surface modification. 31. A. Lee and M. “Nanoparticle-based theranostic agents. P. 203-204.22. “Gold and silver nanoparticles in sensing and imaging: sensitivity of plasmon response to size. 24. Jäckel. De. 19220-19225. 4. Bhattacharya and P. 22. J. A. Bhattacharyya. 1307-1315.

no. 12. Grobmyer. “Nanomedicine for drug delivery and imaging: a promising avenue for cancer therapy and diagnosis using targeted functional nanoparticles. Le Sech and S. no. “Platinum nanoparticles: a promising material for future cancer therapy?. Patra. Bhattacharya. G. R. H. “Targeted photodynamic therapy of breast cancer cells using antibodyphthalocyanine-gold nanoparticle conjugates. 2336-2357.” Small. “Engineering nanocomposite materials for cancer therapy. Furusawa. 363-367. Usami.” Cancer. B. P.” Methods in Molecular Biology. “Emerging implications of nanotechnology on cancer diagnostics and therapeutics. Cance and S. 131. F. 38. vol. Liu. R. pp. 10. 2010. N. Lu. “Potential therapeutic application of gold nanoparticles in B-chronic lymphocytic . N. Abraham. vol. Bone. Stuchinskaya. E. K. M. C.” International Journal of Cancer. A. Vibin. Moreno. Libutti. Kobayashi. Edwards and D. S. 2009. C. Minelli. Wang. Delano. 459-466. M. Nakamura. S. Kumar. 6. 85103. 3. Jiang. Cook.” Photochemical & Photobiological Sciences. M. N. 5. 074001. W. Chandra. “Nanoparticles for thermal cancer therapy. pp. no. Morton and J. vol. A. C. vol. Y. Powell. 5. A Russell. M. 2011. P. S. 41. 2006. 21. Abdelwahab. Hochwald. M. R. N. Paciotti and S. R. K. Shenoi and A. 107. 2010. 37. Mukherjee. P. Secreto. pp. 7. Remita. Yaszemski. pp. Liehn. V. Y. Kay and D. Lee. Cuenca. J. 8. 21. 2010. Miyoshi and M. pp. 36. Raji. 39. N. Porcel. “Gold nanoparticles in molecular diagnostics and therapeutics.” Experimental Cell Research. 40. DAS. T. vol. M. 2010.” Nanotechnology. J. E. C. “Colloidal gold: a novel nanoparticle for targeted cancer therapeutics. C. 2527-2537. G. C. V. vol. pp. J. no. D. K. J. vol. in press. no. 375-384. Rejiya.” Digest Journal of Nanomaterials and Biostructures. H. 2007. pp. S. G. Day.32. 2011. L. pp. Lacombe. S. Lowe and M. West. 35. 624. 33. 2. Mukhopadhyay. L. Stevens. D. Banerjee. A. A. E. H. vol. 34. 120. Y. C. G. no.” Journal of Biomechanical Engineering. S. “Selective photothermal efficiency of citrate capped gold nanoparticles for destruction of cancer cells. no. 822-831.

132. “In vivo tumor targeting and spectroscopic detection with surface-enhanced Raman nanoparticle tags. Langer and D. no. S. L. 5. no. 1998. M. 2009. 6669. A. S. Mello. 563-570. D.” Trends in Biotechnology.” Trends in Molecular Medicine. 47. G. C. 46. Whitehead. “Gold nanopopcorn-based targeted diagnosis. D. vol. A.leukemia (BCLL): enhancing apoptosis. 83-90. Y. A. Singh. no. Y. 391. Ferec. vol. 12. F. no. 2010. A. 44. no. 45. Ansari. C. vol. H. Prigodich. A.” Nature. Couvreur. Qian. C. vol. vol. S. Z. A. Ray. Fu. Driver and C. Yang. 11. 50. vol. A. Mirkin. “Fluorescent metal nanoshell probe to detect single miRNA in lung cancer cell. 2009. “Near-infrared fluorescent nanoprobes for cancer molecular imaging: status and challenges. S. 60. 2072-2073. vol.” Journal of the American Chemical Society. and in situ monitoring of photothermal therapy response of prostate cancer cells using surface-enhanced Raman spectroscopy. 2010. A. pp. M. 82. N. S. S. E. 574-583. Mei. Kostas. N. 48.” Analytical Chemistry. nanotherapy treatment. 18103-18114. Yu and P. D. 42. “Gene regulation with polyvalent siRNA-nanoparticle conjugates. K. vol. no. 26. 9. A. Wang and S. “The potential of oligonucleotides for therapeutic applications. 43. Toub. no. “Innovative nanotechnologies for the delivery of oligonucleotides and siRNA. 24. 2008. Lu. S. Giljohann. O. H. Gao. K. Q. 2006. vol. P. Patel and C. Cheng. He. X.” Biomedicine & Pharmacotherapy. 49. C. 6. 8. pp. Nie. 51. 806-811. 607-620. pp. D. E. Khan. Yin-Goen. 12. 2. D. 2010. 131. pp. no. Young.” Journal of Nanobiotechnology. Gambhir and Z. no. E. pp. Shin. X. Peng. Jiang and J.” Nature Reviews Drug Discovery. X. “Knocking down barriers: advances in siRNA delivery. K. Fire. G. Fichou and C. Y. Senapati. J. Montgomery. . Seferos.” Journal of the American Chemical Society. Xu. 2006. 4. Fattal and P. 16. Anderson. R. 1. pp. D. pp. pp. Lakowicz. Chen. pp. M. J. Malvy. W. 129-138. vol. R. 2007. pp. 4464-4471. Zhang.” Nature Biotechnology. “Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans.

Z. W. 431. J. Missirlis. K. pp. 1. S. 312. Tirrell and N. J. 464. S. R. vol. J. Jiang. “Engineering Aspects of Hyperthermia Therapy. “Gold. L. 2007-2015. 1999. D. poly(beta-amino ester) nanoparticles for small interfering RNA delivery. 57.” Nature. no.” Annual Review of Biomedical Engineering. G. L. M. 9393. no. 60. pp. O. Liang. Klein and P. no. 1. 3. Langer and D. Wu. S. Lee. Zhao. Bae. Anderson. vol. Y.” Lancet. vol. G. 1027-1030. no. Wang. H. R. Wadhwani. 2004. 1. vol. . Gary and M. “Unlocking the potential of the human genome with RNA interference. Shi. Baker.” International Journal of Pharmaceutics. Lee. B. Green. S. vol. Sunshine. 94-101. Dong and X.” Nature. Q. vol. Deng. 53. no. 55. no. “RNA interference in biology and medicine. 7. Rossi. M. C. “RNA interference: From tools to therapies. 2003. pp. pp. R. K. J. “Laser-Activated Gene Silencing via Gold Nanoshell-siRNA Conjugates.” Nanoscape. Giljohann.51. pp. J. 7006. no. 7292. A. S. C. 1401-1403. Roemer. 56. A. S. 2010. vol.” Pharmacological Reviews. Mattson. G. N. 2006. 362. P. vol. “Oligonucleotide-modified gold nanoparticles for intracellular gene regulation. D. Lee and T. 9. Wall and Y. N. Guo. 2008. R. J. 4. H. D. 58. vol. pp.” ACS Nano. 2402-2406. Thaxton. Reich. “Enhanced gene delivery and siRNA silencing by gold nanoparticles coated with charge-reversal polyelectrolyte. 2009. Love. G. 4. 9. 5505-5511. K. “Amine-functionalized gold nanoparticles as non-cytotoxic and efficient intracellular siRNA delivery carriers. 2003. 364. J. vol. Lacor. pp. Sun. 5776. R. H. Q. 7. no. A.” ACS Nano. O. no. 6-10. 52. pp. 629-648. 59. Park. Rosi. A. Huang. S. Y. Liang. G. 6. 347-376. Kim. pp. 2010. 61. J. A. 54.” Science. “Small RNA: can RNA interference be exploited for therapy?. Y. T. 371-378. no. 2009. Mirkin. Braun. Zasadzinski. J. vol. L. 2010. A. “Efficient Gene Silencing in Neural Cells by Functionalized Gold Nanoparticles. 1225. Hannon and J. A. N. 55. Milhavet. Xing. M. Du. Han and C. Pallaoro.” Nano Letters. Lytton-Jean. K. pp. pp. P.

U. 66. S. S. Chen. M. T. Payne and J. E. Zhang. Glazer and S. no. R.” Langmuir. “Gold nanorods in photodynamic therapy. 5. Jordan. T. vol. X. Chen and C. 6.” Journal of the American Chemical Society.” Nano Letters. Jain. 62. S. no. 65. Gneveckow. Kojima. 2006. “Clinical hyperthermia of prostate cancer using magnetic nanoparticles: presentation of a new interstitial technique. H. 171-176. vol. L. P. “Targeted hyperthermia using metal nanoparticles. no. 68.” Methods in Molecular Biology. A. A. vol. 7. Kuo. A. W. Feussner. 7. S. 70. C. 3. J. X. Cherukuri. Y. “Cancer cell imaging and photothermal therapy in the near-infrared region by using gold nanorods. H.” Cancer Letters. Halas.” Advanced Drug Delivery Reviews. 412-417. Li. L. A. vol. “Photothermal tumor ablation in mice using near infrared-absorbing nanoparticles. El-Sayed. West. J. N. Huang. L. vol. “Applications of gold nanorods for cancer imaging and photothermal therapy. Y. no. Li. Z. 624. Yeh. Waldofner. N. Curley. and . H. pp. Siekkinen. no. Huang. 2004. pp. S. H.62. Xia and X. 23. no. M. 2010. 2007. X. I. vol. Harada. Xi. H. Hirsch. Loening and A. 209. A. P. 2. Chang. 67. D. El-Sayed. Johannsen. C. pp. J. 21. 5243-5246. 10. 82. 63. vol. “Preparation of poly(ethylene glycol)-modified poly(amido amine) dendrimers encapsulating gold nanoparticles and their heat-generating ability. Yang. Wang. 128. Haba. 2. 343-357. H.” Photochemistry and Photobiology. R. pp. 339-345. A. P. Ura. as hyperthermia agents. 2005. Deger. “Determination of the minimum temperature required for selective photothermal destruction of cancer cells with the use of immunotargeted gold nanoparticles. Warsen. Chang. S. L. H. vol. J. Wust. A. “Immuno gold nanocages with tailored optical properties for targeted photothermal destruction of cancer cells. Chien. O'Neal. 2006. Y. A. N. pp. D. P. I. Huang. 2115-2120. 2010. 64.” International Journal of Hyperthermia. Eckelt. El-Sayed. Y. A. 1318-1322. J. Au. 2007. K. El-Sayed. 69. D. W. Scholz. no. pp. El-Sayed and M. Kono. Y. Horinaka and K. pp. Qian and M. pp. El-Sayed and M. I. 637-647.

2009. L. E. X. 2011. J. E. N. vol. Skrabalak. 78.” Photochemistry and Photobiology. Chen. vol. Lal. 3. 1929-1934. 71. 72. Cho and P. K. L. S. Xia. Cobley. 2008. “Nanoshell-enabled photothermal cancer therapy: impending clinical impact. 4. 709-711. El-Sayed and M. no. Akchurin. 2007. vol. C. X. in press. vol. Khlebtsov. J. Lee. G. surface conjugation and photothermal effects. 5. Halas. Cheng. Q. Journal of Biomedical Optics. L. Khlebtsov. H.” Accounts of Chemical Research. 79. 2005. 217-228. Lu. pp. pp. Drezek. H. X. vol. England). C. Hirsch. 1012-1014. Zhang. M. El-Sayed. M. N. West and R. L. Y. Halas. Yang. Halas. W. Jain. W. N. vol. 15. pp. no. B. Au. 41. Brown. Li. 23. no. I. “Gold nanoshell bioconjugates for molecular imaging in living cells. H. Wei. Xia. vol.” Angewandte Chemie International Edition. G. 5. L. no. G. I. X. 2010. 7.” Optics Letters. S. “Near-infrared resonant nanoshells for combined optical imaging and photothermal cancer therapy. pp. R. N. 2. pp. James. “Gold nanorods as contrast agents for biological imaging: optical properties. 73. Wei and J. pp. Xia. 7.” Nano Letters. 75. N. J. no. 2711-2715. A. V. no.” Nanomedicine (London. 1. 2008. K. 30. Li and Y. 9. Maslyakova. M. 49. Tuchin. Maksimova and V. 021016. V. . Huang. Lee. J. 76. Halas and R. A. West. A. no. pp. “Plasmonic photothermal therapy (PPTT) using gold nanoparticles. Terentyuk. 77.” Accounts of Chemical Research. 21-32. Q. 74. G. West. 85. 2008. X. M. Clare and N. C. vol. 12. G. Chang. Suleymanova. Drezek and J.in near-infrared optical imaging. M.” Nano Letters. Gobin. "Laser-induced tissue hyperthermia mediated by gold nanoparticles: toward cancer phototherapy". Drezek. Loo. 14. Loo. 657-668. L. S. A. D. no. pp. Tong. “Gold nanocages for cancer detection and treatment. Lowery. P. 1842-1851. “Immunotargeted nanoshells for integrated cancer imaging and therapy. A.” Lasers in Medical Science. 2005. 2009. C. E. N. E. “Gold nanocages: from synthesis to theranostic applications. J. S.

“Tunable plasmonic nanoprobes for theranostics of prostate cancer. E. no. L. E. Y. pp. M. 50. Kanzius. 144. Piuzzi. D. “The in vivo performance of plasmonic nanobubbles as cell theranostic agents in zebrafish hosting prostate cancer xenografts. Elagin. 3. Y. J.2956-2964. S. Huang. vol. 82. 6.” Langmuir. E. pp. 20. vol. Lukianova and A. Geller. “A new photothermal therapeutic agent: core-free nanostructured Au x Ag1-x dendrites. 38. O. 11860-11865. Yeh. vol. 31. J. Cardinal. A. 2006. Zagaynova. “OCT-guided laser hyperthermia with passively tumor-targeted gold nanoparticles. Delk. J. O. H. 2011. 2008. vol. R. S. Farach-Carson and D. “Comparative efficiencies of photothermal destruction of malignant cells using antibody-coated silica@Au . 2003. 81. pp. 83. M. Yeh. Shenefelt. V.80. 718-727. J. 87. C. W. vol. M. Bernardi. M. V. 14. Lapotko. Wagner. 125-132. R. L. 86.” Theranostics. FarachCarson and D. “Selective laser nanothermolysis of human leukemia cells with microbubbles generated around clusters of gold nanoparticles. A. F. A. O. Y. 7567-7574. A. V. 3. 85. J. Shieh and C. Huang.” Biomaterials.” IEEE Transactions on Bio-medical Engineering. C. C. Snopova. Hafner. “Noninvasive radiofrequency ablation of cancer targeted by gold nanoparticles. Hafner. 84. N. 29. no. Sefah. A. 2008. Oraevsky. vol. pp. Oginsky. Pisa and E. Lukianova-Hleb. K. P. C. Lapotko. N. no. T. S. D. Lukianova-Hleb. 24. no. Sirotkina. 3-17. Chang and W. Y. W. Shirmanova.” Surgery. O. pp. Chory. Bugrova. S. Nalesnik and D. “Selective photothermal therapy for mixed cancer cells using aptamer-conjugated nanorods. 2. H. C. B. D. V. “Specific absorption rate and temperature elevation in a subject exposed in the far-field of radio-frequency sources operating in the 10-900-MHz range. 631642. V. Kamensky. 2010. M. S. vol. N. Klune. Bamrungsap. P. no. Denisov and E. C. Nadtochenko. A. 2008. 10. L. S. Lapotko. Cheng. E. Su. A. no. V. S. B. Wagner. K.” Journal of Biophotonics.” Lasers in Surgery and Medicine. A. 2010. 1. Jeyabalan. T. G. H. 295-304. D. Chen and C. pp. Tan. Hu. Samaniego. 88.” Chemistry. Cavagnaro. no. 10-11. J. M. vol. F. M. D. pp. Hwu. pp.

Venugopal. J. Daniel. S. Zubarev. 14652-14653. vol. no. B. “Application of nanotechnology in cancer research: review of progress in the National Cancer Institute's Alliance for Nanotechnology.” Journal of the American Chemical Society. W. 94. 2009. Lin. E. Graham and N. W. 2009. . Mirkin and S. hollow Au/Ag nanospheres and Au nanorods. J. 19194– 19201. A. 89. Ehdaie. M. vol. pp. no. pp. 95. Mohammad. pp. pp. R.” Nanotechnology. A. 10. 3. P. L.nanoshells. R. Gibson. 108-110.” Journal of the American Chemical Society. 114. C. Flint. Brown. Kim. 37. D. Stirling. 42. Wheate. “Gold nanoparticles for the improved anticancer drug delivery of the active component of oxaliplatin. P. Nativo. Rajh. 2007. M. T. 2010. 6668. R. vol. IEEE Transactions on Magnetics. Hwu. no. Y. Rozhkova. D. Y. 41. 45. R. 132 . 4678-4684. C. 131. J. S. 4821-4824. 129. J. B. "Synthesis of Hybrid Gold/Iron Oxide Nanoparticles in Block Copolymer Micelles for Imaging. D. B. Yeh. Plumb. S. H. Bader and V. J. no. 2009. pp. D. “Polyvalent oligonucleotide gold nanoparticle conjugates as delivery vehicles for platinum(IV) warheads. Journal of Physical Chemistry C. Hsu. J. D. A. no. Josephrajan. 93. no. 11653-11661. 2007. 90. Giljohann. pp. S. H. R. Dhar. and Magnetic Hyperthermia". Cheng.” International Journal of Biological Sciences. 2010. 20. Weber. S. D. vol. T. 92. Kumar. C. A. 2. B. D. F. 2009. P. Novosad. Lippard. Edwards. Vol. vol. 13.” Journal of the American Chemical Society. vol. “Targeted Paclitaxel by conjugation to iron oxide and gold nanoparticles. Smith. D. Khanal and E. J. 1. 425104. A. A. Drug Delivery. 45. 91. S. pp. no. "Influence of Gold Nanoshell on Hyperthermia of Superparamagnetic Iron Oxide Nanoparticles".” Journal of the American Chemical Society. Uppu and C. Shieh. G. Balaji. pp. no. Su and D. S. F. “Paclitaxel-functionalized gold nanoparticles. vol. 131.

vol. X. Nanomedicine and Nanobiotechnology. Jiang. no. H. “Estimation of tumour dose enhancement due to gold nanoparticles during typical radiation treatments: a preliminary Monte Carlo study. Suh and J. H. 8. Gu.” Journal of the American Chemical Society. 95-99. no. pp. J. H. Z. Kim. Xu. N163-173. 1. 2. 13. J. 461-477. J. . Kong. pp. Lee. Huh. pp. L. 157-184. vol. 2008. 1537-1543. 51. X. no. Fruchard. J. “Ag nanoparticles sensitize IR-induced killing of cancer cells. Biology. Kneipp. 293-298. 2005. 24. vol.” Small. J. Sershen. 4. X. 5. J. Cho. Y. vol. Wang. X. 7661-7665. vol.” Physics in Medicine and Biology. Li. Chen. Chen. H. R. vol. pp. Wang. C.” Cell Research. H. S. P. Zhang and N. Wittig and K. R. T. Gu. J. 97. no. M. X. Cho. Y. Vartholomeos. P. H. 2010. W. Sun. W. 2010. pp. 2000. 102. J. Park. vol. Westcott. “Novel optical nanosensors for probing and imaging live cells. “Artificially engineered magnetic nanoparticles for ultra-sensitive molecular imaging. Yang. Guo. 214-226. E. Zeng. J. Jeong and S. B. 2007. 98. L.” Wiley -Interdisciplinary Reviews. 103. “Enhancement of radiation cytotoxicity in breastcancer cells by localized attachment of gold nanoparticles. Y. Jang. T. “Near infrared imaging with nanoparticles. no. 100. H. 3. J. Halas and J. Altinoğlu and J. Adair. T. Yoon. J. S. Y. vol. Xing. Seo. 2009. S. Kneipp. Kneipp. Ma. Yang. no. West. McEwan. and Medicine. S. G. 15. 9. J. 104. no. S. Jon. Huang. L. “MRI-guided nanorobotic systems for therapeutic and diagnostic applications.” Nature Medicine. “Temperature-sensitive polymer-nanoshell composites for photothermally modulated drug delivery. vol. J. 1031-1034. Z. E. S.” Nanomedicine: Nanotechnology. no. 101. D. Jun. Lee. Cheon. W. 13. M. Kim. Y. I. 19. 2007. pp. Z. Fan. Chen and J. 99. Liu. J. Wang. Roa. Song. S. McQuarrie. Y. 2. Y. 2011. pp. 129. pp. A. Ferreira and C. M.96.” Annual Review of Biomedical Engineering.” Journal of Biomedical Materials Research. 50. Mavroidis. A. pp. N. “Antibiofouling polymercoated gold nanoparticles as a contrast agent for in vivo X-ray computed tomography imaging. 6. X.

K. Yang. T. T. 12. 4. Y. C. no. C. Y. Nanomedicine and Nanobiotechnology. C. pp. Kiang. Kim. H. Wang. 21. Kah. K. “Control of optical contrast using gold nanoshells for optical coherence tomography imaging of mouse xenograft tumor model in vivo. Wu. 4995-5009. Ralston. 29. 16. J. Lee. S. N. pp. Brenner and E. A.” Recent Patents on Nanotechnology.” Journal of Materials Chemistry. A. no. “Imaging gold nanorods in excised human breast carcinoma by spectroscopic optical coherence tomography. V. no. 360-368. C. T. 112. no. 2009. pp. vol. 295102. 15. J.” Journal of Biomedical Optics. pp. Z. vol. M. V. P. J. B. vol. no. Park. Y. Jeong and S. J. H. B. D. S. 106. Y. V. A. 6407-6411. M. M. 2277-2284. V. 108.” Trends in Molecular Medicine. 561-573. J. vol. Balalaeva. S. “Contrasting properties of gold nanoparticles for optical coherence tomography: phantom. Song. 2010. E. M. Tseng. Yu. pp. E. 110. Welch and Y. D. Bugrova. . in vivo studies and Monte Carlo simulation. vol. 357. “Computed tomography . 2009. Orlova. “Inorganic nanoparticlebased contrast agents for molecular imaging. N. 2008. Olivo. D. Kamensky. 054015. 109. Agrba and V. pp. S. S. A. Chow. Hall. 53. Wei and S. 22. vol. 113. T. C. X. pp. J. vol. J. W. Khlebtsov. Ashkenazi and L. W. Chou and C. 107. Glaus. J. 1. 171-180. 19. Jon. Zagaynova. Lee. Shirmanova. Y. 2010. Y. C. vol. 14. K. S. Wu. 2007. P. Boppart. pp. Chen. M. A. Y. 18. 2010. E. D. Wang. J. no.105. M. pp. M. no. M. Yang. Chi. A. Koh. T.” Physics in Medicine and Biology. L. K. H. 3. Xia. C. M. Stein. M. 2011. Mhaisalkar and C. “Nanoparticles for photoacoustic imaging. G.an increasing source of radiation exposure.” Nanotechnology. 155101. “Au nanorings for enhancing absorption and backscattering monitored with optical coherence tomography. no. L. 4. “Nanoparticles for improved therapeutics and imaging in cancer therapy. 5. vol. Sirotkina. I. Tsai. Y.” The New England Journal of Medicine. Kirillin. “Amphiphilic polymer-coated hybrid nanoparticles as CT/MRI dual contrast agents. Y. 2009. Oldenburg. 22. Hansen. T. Chithrani. Cho.” Wiley Interdisciplinary Reviews. 111. Chiang. K.” Nanotechnology. Sheppard. Yang.

” Nano Letters. Lewinski. V. 123. 2008. “Photoacoustic tomography of a nanoshell contrast agent in the in vivo rat brain. Johnston and T. K. C. K. Kuranov. O'Neal. Sokolov. M. Feldman. Wang.” Biomedical Optics Express. 2010. Xia. Olmedo. A. 1689-1692. Ma. J. Baranov. vol.114. M. Soto. 7. 120. V. V. 1. Wang. Kneipp. vol. Y. I. S. Conjusteau and M.” Nanoscale Research Letters. A. 115. Barria. J. Gill. Y. pp. no. Hung. 2010. Chen. vol. “Immunological properties of engineered nanomaterials. Paranjape. E. no. M. pp. “Noninvasive in vivo spectroscopic nanorod-contrast photoacoustic mapping of sentinel lymph nodes. L. K. “Assessment of the In Vivo Toxicity of Gold Nanoparticles. “In vivo molecular probing of cellular compartments with gold nanoparticles and nanoaggregates. pp. Kim. “Enhanced multi-spectral imaging of live breast cancer cells using immunotargeted gold nanoshells and two-photon excitation microscopy. J. P. vol. vol. Kogan and C. 119. Song . A.” Nanotechnology. McLaughlin. Vergara. Sun. T. 31. D. D. Stoica and L. Oraevsky. I. A.” Nature Nanotechnology. Drescher and J. L. 3259-3269. 19. P. J. 1914-1918. pp. pp. Milner. M. Bickford. 8. 2. Liau and G. 2009. 116. Wang. V. “Surface-enhanced Raman scattering hybrid nanoprobe multiplexing and imaging in biological systems. 315102. C. K. 2-16. C. Fu. “High sensitivity of in vivo detection of gold nanorods using a laser optoacoustic imaging system. 118. 858-864. 122. 70. 7. 2007. 4. Kotov. no. N. Gonzalez-Romero. 2009. 1. pp. N. S. Dobrovolskaia and S. 2. X. L. E. Kneipp. Clos. 2006. X. no. R. L. A.” Nano Letters. D. “Depth resolved photothermal OCT detection of macrophages in tissue using nanorose. Y. Huang. Ku. Drezek. Chang and R. pp. 2004. 2007.” Nano Letters. Brown and K. vol. Urayama. Wang. “Bioaccumulation and toxicity of gold nanoparticles after repeated administration . Eghtedari. Nammalvar. vol. 117. J. G. K. D. H. D. pp. Matschulat. A. K. pp. M. no. Maslov and L. Villard. Wang. no. McNeil. M. S. 4. Lasagna-Reeves. H. 10. A. A. W. 8. 4. A. 6. Sadagopa Ramanujam. 469-478. M. J. vol. 2225-2231. Kneipp. G. Copland.” ACS Nano. no.” European Journal of Radiology. vol. Kneipp. 121. S. no. V. 6. A. Motamedi. 227-231. L.

M. 1. E. pp. G. 4. 3.” Nanomedicine (London. no. no. S. B. Hande and S. 2581-2588. Y. L. “Smart polymeric carriers for enhanced intracellular delivery of therapeutic macromolecules. A. Huang and M. no. pp. S. Hackenberg. Mwamuka. K. E. 23-32. England). 125. 1941-1949. Ye. 5996-6003.” Nano Letters. 126. S. C.” Biomaterials. pp. Y. Neuss. 2011. Li. C. 130. 5. Simon. Pan. B. 2010. no. H. pp. N. pp. S. no. no. Hummel. vol. 2008. vol. 2007. Yung. S. 5. El-Sayed. A. “Autophagy and oxidative stress associated with gold nanoparticles. 5. 124. Froelich. 127. Kessler. J.” Biochemical and Biophysical Research Communications. Ren. M. X. W. Gole. S. Leifert.” Expert Opinion on Biological Therapy. M. 7. X. Xinyi. Murphy and M. 2005. Schmid. “DNA damage and p53-mediated growth arrest in human cells treated with platinum nanoparticles. Technau. C. L. no. pp. S. 1. 19. A. 11. toxicity and functional impairment in human mesenchymal stem cells. P. P. K. no. Stayton. P. 1. J. pp. 3. 5. D. L.” Journal of Materials Science: Materials in Medicine. N. Sun. Wyatt. “Size-dependent cytotoxicity of gold nanoparticles. D. Rotello. F. 2010. C. Ginzkey. C. J. “Silver nanoparticles: evaluation of DNA damage. no. Q. Scherzed.” Toxicology Letters. J. 1. Ghosh. vol. C. Valiyaveettil.in mice. Hoffman and P.” Small. Huang. Asharani. 2005. 393. Kim. pp. J. P. Menichetti and V. vol. “Gold nanoparticles are taken up by human cells but do not cause acute cytotoxicity. F. 829-834. Bay and L. H. Koehler. Connor.” Small. Pagliuca. M. 2005. Zhang. Wen. A. “In vivo toxic studies and biodistribution of near infrared sensitive Au-Au(2)S nanoparticles as potential drug delivery carriers. Q. El-Sayed. Jahnen-Dechent. Zhu. vol. M. 128. vol. A. Fischler. Z. vol. 649-655. E. vol. “Surface plasmon resonance scattering and absorption of anti-EGFR antibody conjugated gold nanoparticles in cancer diagnostics: applications in oral cancer. Hagen and N. 325-327. R. Ong. Kleinsasser. vol. A. M. 27-33. V. 129. 23. Tan and G. “Entrapment of hydrophobic drugs in nanoparticle monolayers with efficient . C. 31. 131. 132. 51-64. El-Sayed. Zhang. M. I. Brandau and W. Hartono. Chow. 201. U. pp. 2010.

Wang. vol. 4. F. C. 140.” Journal of Nanoscience and Nanotechnology. Schlager. D. Hussain. vol. R. H. 11. 30. pp. no. M. M. Powell. 141. Qiu. L. 138. A. Griffin. no. pp. B. Gearhart. in press. C. Autrup. E. 7606-7619. 2006. K. Pavel. Liu. 145-169. T. 19. S. 1014-1020. J. 131. 137. 2010. Tamarkin. Tian. 15531561. vol. L. 2. H. Sun. “Comparative in vitro cytotoxicity assessment of some manufactured nanoparticulate materials characterized by transmission electron microscopy.” Toxicological Sciences. R. Y. 139. N. 975-983. K. Chen. “Cytotoxicity and genotoxicity of silver nanoparticles in the human lung cancer cell line. K. W. Murr. Toxicology In Vitro. A. R. D.release into cancer cells. 4. Bischof. K. 88. “Cytotoxicity and immunological response of gold and silver nanoparticles of different sizes. pp. H.” Small. R. pp. L. Garza and L. N. C. J. 2005. M. no. 2004. vol. Xu. vol. J. 412-419. Zhang. Y. “Surface chemistry and aspect ratio mediated cellular uptake of Au nanorods. Paciotti. McLaughlin and L. Dang and H. 2-3.” Drug Delivery. vol. Hofmann. M. “In vitro cytotoxicity of nanoparticles in mammalian germline stem cells. 3. Y. Ebbini. D. S. Paciotti. Wang. Hsu and C. E. Carrasco.” Journal of Nanoparticle Research. “In vitro toxicity of nanoparticles in BRL 3A rat liver cells”. X. 1210-1216. 13. 136. L. 2009. Ji. Y. Zhao. 135. Geiss and J. no. 2005. Wu. Foldbjerg. C. J. G. Y. Song and J. Bai. 2011. no. Goia. 2009. pp. Li and C. no. 2. T. A549. pp.” Molecular Cancer Therapeutics. no. K. S. 11. Hussain. pp. Myer. J. W. R. “Enhancement of tumor thermal therapy using gold nanoparticle-assisted tumor necrosis factor-alpha delivery. 133. Williams. Y. “Colloidal gold: a novel nanoparticle vector for tumor directed drug delivery. G.” Archives of Toxicology. 7. F. Yen. L. 5. Braydich-Stolle. . Hess. S. Schlager and M. 7.” Journal of the American Chemical Society. L. Soto. pp. 31. X. E. 2010. Tsai. Ren and X. Weinreich. L. pp. vol. no. vol. G. vol.” Biomaterials. 169-183. 134. Visaria. “Shape dependence of gold nanoparticles on in vivo acute toxicological effects and biodistribution. no. 5. D. F. J. 1360-1361. 2005.

pp. no. 4. . 1. 5. 43-54.142. Asharani. Gong and S. 2011. Bellucci. Valiyaveettil. vol. “Nanoparticles and Nanodevices in Biological Applications. pp.” Lecture Notes in Nanoscale Science and Technology. P. Lianwu. “Comparison of the toxicity of silver. S. Z. 143. gold and platinum nanoparticles in developing zebrafish embryos. V. vol. Y.” Nanotoxicology. 2009. 1-198.