Professional Documents
Culture Documents
net/publication/346579168
CITATION READS
1 170
2 authors:
Some of the authors of this publication are also working on these related projects:
Development and evaluation (invivo and invitro) of liposomal cream by using flax seed oil and tamarind oil against ageing View project
All content following this page was uploaded by Aditya Singh on 03 December 2020.
ABSTRACT
There are many issues with traditional drug supply networks, and most work has now moved from synthetic to
herbal medicines. Therefore, it would be a safer choice to switch to healthy, reliable and tested Ayurvedic herbal
medicines. Owing to the large variety of bioactive molecules and their higher safety margin, this is possible the
active component of the family Tamarind Indica (Tamarind), is based on this study. Oils are volatile in nature and
separated from the plant by plant organs such as seed. Liposomes encapsulating essential oils are promising agents
to treat topical diseases used useful in topical delivery which heal and treat acute and chronic diseases. As a
supplementary medicinal device, plant oils have also proven useful. Liposomes are targeted modified drug carrier
system which contains both water-soluble drug as well as oil-soluble drug. Liposomes are formulated by
cholesterol and natural nontoxic phospholipids. The concept of topical drug delivery emerged from the desire to
provide patients with more convenient means of taking their medication. The purpose of developing a dosage form
for a very quick onset of action, which is very convenient for the administration.
Keywords: Extraction, herbal, liposomes, encapsulation, antiaging activity.
Fig.1: Complete assembly for extraction of tamarind seed oil having Soxhlet Apparatus; round bottom
flask on heating mantle
938| International Journal of Pharmaceutical Research | Jul - Sep 2020 | Vol 12 | Issue 3
Aditya Singh et al / Extraction, Development, and Characterization of Tamarind Seed Oil Based Liposome
[A] [B]
Fig.2: Separation of Tamarind Seed oil by using Rotatory Evaporated[A] Rotatory evaporator, [B]
Tamarind seed oil
Formulation of Liposome with handshaking method tamarind oil were dissolved in to 5ml of
All three composition in a ratio 1:1:1 [cholesterol: chloroform[14]. Then transferred in to Round
soya lecithin :drug] were taken. 1gm of cholesterol bottom flask with proper handshaking for 1hour.
and 1 gm of soya lecithin were weighed and When thin layer deposit into the wall of RBF than
dissolved with 10 ml of chloroform with hydrated with buffer pH 6.8[15]. Liposome was
continuously mixing by using glass rod then 1ml of prepared and collected.
[A] [B]
Fig.3: [A] Process of Liposome by handshaking method [B] Liposome
Evaluation Parameter Integrated output (percentages) is the percentage of
Microscopy analysis- Liposomes were analyzed by total product quantity in the final wording. The
using microscope and images were taken to efficiency of incorporation is determined using the
examine microscopical structure of prepared following equation: [ (T-S)/T ] x100, where T is the
liposomes. total amount of oil in both the supernatant and the
sediment, S is that amount of oil found in the
Determination of Rheological properties[16]
supernatant obtained after ultra-centrifugation.
By the help of Brookfield viscometer the viscosity
Encapsulation efficiency is usually derived from
was determined 4, 8, 12 at 30 rpm, 60rpm, and
spectrophotometric methods.
90rpm for 1 min at room temperature.
Zeta potential studies [21]
pH [17]
The Zeta potential of an particle is known as the
The weight and dissolution was approx. 0.5 g of the
total charging of a particle in a particular medium,
topical preparation in 50 ml distilled water and its
and a zeta potential calculation for colloidal
pH was measured.
structures can be used if the stability of the particle
Homogeneity [18] is lower than zeta is zero.
With the help of visual appearance and touch the
In vitro Diffusion studies [22]
homogeneity was tested.
By using Franz cell diffusion or egg membrane to
Appearance [19] perform the diffusion study by using buffer take at
The appearance was judged by its colour, least 6 samples for dilution study. 1 ml sample and
roughness and graded. 10 ml buffer 6 times per 10 mint.
Encapsulation efficiency [20]
RESULTS
939| International Journal of Pharmaceutical Research | Jul - Sep 2020 | Vol 12 | Issue 3
Aditya Singh et al / Extraction, Development, and Characterization of Tamarind Seed Oil Based Liposome
…
[A] [B] [C]
Fig.4: Microscopic image of liposomes at [A] 1st day [B] 2nd day [C] 3rd day
Calibration curve of Tamarind seed oil
Table 1: Standard Calibration Curve data of Tamarind oil
Concentration(µg/ml) Absorbance
0.25 0.0155
0.5 0.0682
0.75 0.2069
1 0.3081
1.25 0.4359
940| International Journal of Pharmaceutical Research | Jul - Sep 2020 | Vol 12 | Issue 3
Aditya Singh et al / Extraction, Development, and Characterization of Tamarind Seed Oil Based Liposome
Formulation [F]
Hrs. % release
1 18.60%
2 23.70%
3 28.25%
4 31.30%
5 37.10%
6 44.45%
[A] [B]
Fig.5: [A] Zeta potential [B] SEM image
DISCUSSION 2. Bakkali F, Averbeck S, Averbeck D, Idaomar M.
1. Drug entrapment was found to be 68.40%. Biological effects of essential oils-A review. Food
2. Invitro drug released was found to be 44.45%. Chem Toxicol. 2008; 46:446-75.
3. pH was found to be nearly 6.8 which is neutral. 3. Chami N, Chami F, Bennis S, et al. Antifungal
4. Liposomes were found to stable under cool treatment with carvacol and eugenol of oral
temperature. candidiasis in immunosuppressed rats. Braz J
5. Zone of Inhibition was found to be 19.24 mm Infect Dis. 2014; 8:217-26.
after 24 hrs. 4. Boukhris M, Bouaziz, M, Feki I, et al.
6. The spreadability was found to be 13.33 Hypoglycemic and antioxidant effects of leaf
gm.cm/sec. essential oil of Pelargonium graveolens L’Her. In
alloxan induced diabetic rats. Lipids Health Dis.
CONCLUSION 2012; 11:81.
The development of Tamarind seed oil-based 5. Esmaeili A. Biological activities pf Eremostachys
laevigata Bunge. Grown in Iran. Pak J Pharm.
Liposomes is to target so many applications like to
2012; 25:803-8.
treat the aging problems and provide the
6. Cristani M, D’Arrigo M, Manadalari G, et al.
antioxidant activity in topical preparations. Essential
Interaction of four monoterpenes contained in
oils are used by making the modified drug delivery
essential oils with model membranes:
in the form of liposomal formulation enhances its implications for their antibacterial activity. J Agric
activity and also improves its stability problem. Food Chem. 2007; 5(5):6300-8.
Sometimes essential oils also work like a carrier 7. Weisheimer V, Micron D, Silva CB, et al.
which helped to reach the drug at a particular and Microparticles containing lemongrass volatile oil
a targeted site. preparation, characyerization and thermal
Conflicts of Interests stability. Pharmazie. 2010; 6(5):885-90.
The authors declare no conflict of interest. 8. Aliva-Sosa R, Palou E, Jimenez Munguia MT, et al.
Antifungal activity by vapour contact of essential
REFERENCES oils added to amaranth chitosan or starch edible
1. Ajayi I.A., Oderinde., R.A., Kajogbola, D.O., films. Int J Food Microbiol.. 2012; 15(3):66-72.
Uponi J.I.Oil content and fatty acid composition 9. Lertsutthiwong P, Rojsitthisak P.Chitosan-
of someunderutilized legumes from Nigeria. alginate nanocapsules for encapsulation of
Food Chemistry. 2006; 99:115-120. turmeric oil. Pharmazie. 2011; 66:911-15.
941| International Journal of Pharmaceutical Research | Jul - Sep 2020 | Vol 12 | Issue 3
Aditya Singh et al / Extraction, Development, and Characterization of Tamarind Seed Oil Based Liposome
10. Gulati M, Grover M, Singh S, Singh M. Lipophilic Delivery Systems American Chemical Society.
drug derivatives in liposomes. Int J Pharm. 1998; 1993:42-52.
16(5):129-68. 17. Kirby C, Gregoriadis G. Dehydration
11. Bangham A., Standish M.M., Watkins, J. Diffusion Rehydration Vesicles: A Simple Method for High
of univalent ions across the lamellae of swollen Yield Drug Entrapment in Liposomes. 1984; 2:
phospholipids. Journal of Molecular Biology.1965; 979-984.
13: 238-252. 18. Ward PA. Oxidative stress: acute and
12. Torchilin, V, Weissig, V. Liposomes: A Practical progressive lung injury. Animals of the New
Approach. Oxford University Press: Kettering, York Academy of Science. 2010; 1203: 53-59
UK, 2003; pp.77-101. 19. Samad A, Sultana Y, and Aquil M. Liposomal drug
13. Vemuri S, Rhodes CT. Preparation and delivery system update review. Current Drug
characterization of liposomes a therapeutic Delivery. 2007; 4: 297-305.
delivery system: a review. 20. Garg G, Saraf S, Saraf S. Cubosomes: An
PharmaceuticaActaHelvetiae. 1995; 70(2): 95- overview. Biological & Pharmaceutical Bulletin.
111. 2007;30:350-3.
14. Khan I, Elhissi A, Shah M, Alhnan MA, Waqar A. 21. Gendler E. Treatment of the ageing face.
Liposome based carrier systems and devices Dermatology Clinics Fali godina.1998;5:561-7.
used for pulmonary drug delivery. In: DAVIM JP 22. Kligman D. Cosmeceuticals. Dermatology
(ed.) Biomaterial and medical tribology research Clinics. 2009; 18:609-15.
and development. 2013; pp. 395-443. 23. Yasar, Mustafa, and . 2019. The remember
15. Khan I, Yousaf S, Subramanian S, Alhnan M A, regeneration therapy method: An overview of
Ahmed W. Proliposome Powders for the new therapy protocol to approach
Generation of Liposomes: the Influence of diseases. Journal of Complementary Medicine
Carbohydrate Carrier and Separation Research, 10 (1), 68-
Conditions on Crystallinity and Entrapment of a 80. doi:10.5455/jcmr.20181229122909
Model Antiasthma Steroid. AAPS PharmSciTech. 24. Jargin, Sergei V, and . 2019. Drugs and dietary
2007; p.1-13. supplements with unproven effects in research
16. Brannon Peppas L. Controlled Release in the and practice. Journal of Complementary
Food and Cosmetics Industries in Polymeric. Medicine Research, 10 (1), 27-
37. doi:10.5455/jcmr.20181223075028
942| International Journal of Pharmaceutical Research | Jul - Sep 2020 | Vol 12 | Issue 3