Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/387377
Title: Formulation Development and Evaluation of Poly herbal Formulation for Pulmonary Tuberculosis
Researcher: Martolia, Jaya
Guide(s): Tandel, Falguni B
Keywords: Anti-tubercular activity
Clinical Pre Clinical and Health
HPLC
Medicinal Plants
Pharmacology and Pharmacy
Pharmacology and Toxicology
Polyherbal Chewable Tablet
Quality by Design
Standardization
Tuberculosis
University: Parul University
Completed Date: 2022
Abstract: Background: Globally tuberculosis is an extensive health issue and main query with the available treatment is adverse effects and drug resistance. Since ages, Ayurvedic and herbal medicines have to struggle with modern medicines, which are demonstrate to be immediate-acting, strong and newline potent. The evolution in herbal drug formulations and its standardization are intricate and associate with a number of trials. Aim: The present study aims to design, development of an anti-tubercular polyherbal chewable tablets and its standardization and in-vitro anti-tubercular activity. Methods: Based on the literature survey, four anti-tubercular plant extracts i.e. Glycyrrhiza glabra (Yastimadhu), Piper longum (Pippali), Curcuma longa (Haridra), and Adhatoda vasica (Vasaka) were selected for the development of polyherbal chewable tablet formulation. 32 factorial design newline was applied for formula optimization. Tablets were prepared by wet granulation method and quantitatively evaluated by HPLC. In-vitro anti-mycobacterial activity was performed by agar well diffusion method and MGIT BACTECH. Results: Extracts were authenticated by qualitative HPTLC fingerprinting in comparison with suitable raw herbs and phytomarkers. The pre-compression and post- compression studies showed that the formulation F5 showed better taste and good results among all the formulations designed. Quantification by HPLC revealed that polyherbal chewable tablet showed 1.03 % of glycyrrhizin, 0.44 % of piperine, 1.37 % of curcumin, and 0.086 % of vasicine content. Polyherbal chewable newline tablet were stable throughout the stability study (40ºC 2ºC and 75 % 5 % RH). Polyherbal newline chewable tablet showed maximum 22mm to 23mm of zone of inhibition on Mycobacterium newline smegmatis. In-vitro activity on Mycobacterium tuberculosis and MDR tuberculosis strain showed no growth at tested sample compared with positive and negative control.
Pagination: 152
URI: http://hdl.handle.net/10603/387377
Appears in Departments:Department of Pharmacognosy

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01_title.pdfAttached File120 kBAdobe PDFView/Open
02_declaration.pdf108.99 kBAdobe PDFView/Open
03_certificate.pdf276.96 kBAdobe PDFView/Open
04_acknowledgement.pdf14.43 kBAdobe PDFView/Open
05_content.pdf42.68 kBAdobe PDFView/Open
06_list of figures and tables.pdf371.28 kBAdobe PDFView/Open
07_abstract.pdf15.82 kBAdobe PDFView/Open
08_chapter 1.pdf667.13 kBAdobe PDFView/Open
09_chapter 2.pdf463.7 kBAdobe PDFView/Open
10_chapter 3.pdf1.57 MBAdobe PDFView/Open
11_chapter 4.pdf3.05 MBAdobe PDFView/Open
12_references.pdf488.24 kBAdobe PDFView/Open
13_annexures.pdf5.85 MBAdobe PDFView/Open
80_recommendation.pdf403.9 kBAdobe PDFView/Open
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