Professional Documents
Culture Documents
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• To examine the quality of the various
brands of pharmaceutical products, these
products should be evaluated by
• Chinese herbal pharmaceutical observation of outer appearance, particle
product Jia-Wei-Xiao-Yao-San is size, solubility, and the contents of crude
made by various manufacturers, and fiber by using the following methods:
there are different amounts of
various raw herbal powders that are • scanning electron microscope (SEM)
added to the herbal pharmaceutical • light microscopy photographs of Congo
product. red stained
• solubility test
• crude fiber analysis sand crude fiber
(content were not consistent in the herbal
pharmaceutical products.)
A study develops several chemical and physical methods to evaluate the quality of a
traditional Chinese formulation, Jia-Wei-Xiao-Yao-San.
The results demonstrate that the contents of the herbal ingredients of saikosaponin A,
saikosaponin D, ferulic acid, and paeoniflorin were around 0.351 ± 0.017, 0.136 ± 0.010,
0.140 ± 0.005, and 2.281 ± 0.406 mg/g, respectively, for this herbal pharmaceutical product.
The physical examination data demonstrate that the raw herbal powder had rough,
irregular, lumpy, filamentous, and elongated shapes, as well as strong Congo red
staining.
1. Protocol and registration 3. Inclusion criteria for study selection
• Registered on international • Types of study
prospective register of systematic • Randomized Controlled Trial (RCT)
review (PROSPERO). Registration • Types of patients
number : CRD 42019127326. • Clear diagnosis of insomnia.
• Age and gender of the patients are
2. Ethic approval not limited.
• No clinical trials • Types of interventions
• Research data is from published • Experimental group was treated
papers. with Xiaoyao dan alone or combined
• The result will be submitted to a peer- with Western medicine.
reviewed journal.
4. Data collection and management 5. Assessment of risk of bias in
• Randomized method included studies.
• Random concealment • Random sequence generatio
• Sample size • Random allocation concealment
• Number of cases in each group • Blind method implementation
• Age • Outcome assessor
• Gender • Result data integrity
• Condition • Selective outcome report
• Diagnostic criteria
• Blindless 6. Measures of treatment effect
• Blinded subjects • For dichotomous data, 95%
• Experimental group confidence intervals
• Control group interventions • For continuous data, 95%
• Follow up confidence intervals
• Outcomes
• Adverse events
7. Dealing with missing data
• If the literature data being searched is incomplete or ambiguous, the researcher
will contact the author via email or telephone to refine the literature data. If
necessary, the articles will be excluded.
8. Assessment of heterogeneity
• A random effect model was used when there was significant heterogeneity
between trials (defined as P<.1), whereas a fixed effect model was used, and
the I2 test would be used to assess the heterogeneity of the included studies.
• I2 > 50 would be considered high. Indicator of
• heterogeneity.
• When heterogeneity is observed, we will perform a subgroup analysis to
explore possible causes.
• A total of seven ingredients from XYS could act on these hub genes
and they were identified through ultra-high-performance liquid
chromatography-quadrupole time-of-flight mass spectrometry
(UPLC-Q/TOF-MS), including paeoniflorin, quercetin, luteolin,
acacetin, aloe-emodin, Glyasperin C, kaempferol.
https://www.heathmontchinesemedicine.com.au/product/jia-wei-xiao-yao-san/
https://www.verywellhealth.com/xiao-yao-wan-88943
https://pubmed.ncbi.nlm.nih.gov/31035044/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3159992/
https://www.hindawi.com/journals/ecam/2013/952796/