Ali Waris, Shaikh Hamiduddin, Ansari Abdullah, Khanam Salma
Department of Ilmul Saidla (Unani Pharmacy), National Institute of Unani Medicine, Bengaluru, Karnataka, India.
Department of Pharmacognosy, Al-Ameen College of Pharmacy, Bengaluru, Karnataka, India.
Pharmacognosy Res. 2016 Apr-Jun;8(2):147-52. doi: 10.4103/0974-8490.175611.
Quality control of Unani polyherbal formulations is the need of the day for better acceptance of Unani medicine. Qurse Tabasheer (QT) is a Unani polyherbal formulation containing six ingredients, Tabasheer (Siliceous concretions) (Bambosa arundinaceae Retz.), Gule Surkh (Rosa damascena Mill. flower), Gulnar (Punica granatum Linn. flower), Tukhme kahu (Lactuca sativa Linn. seed), Tukhme khurfa (Portulaca oleraceae Linn. seed), and Gile Armani (bole) widely used in treatment of diabetes. The present study was taken up to scientifically evaluate the various physicochemical parameters to standardize the formulation.
To evaluate various physicochemical parameters including ash values, moisture content, extractive values, thin layer chromatography (TLC) and high-performance TLC (HPTLC), friability, disintegration, uniformity, and weight variation for standardization of QT.
Ingredients were identified by the experts. The method mentioned in national formulary of Unani Medicine with modification was followed for preparation of the tablets. Physicochemical standards were established for ideal batch of tablets on the basis of set parameters regarding friability, hardness, and disintegration. Various parameters such as organoleptic characters, extractive values for the extract and HPTLC fingerprinting postcompression were carried out for evaluation of QT.
Parameters for loss of weight on drying, pH, ash values, extractive values documented. Qualitative chemical tests indicated the presence of alkaloid, glycoside, tannins, and steroids. TLC and HPTLC fingerprinting studies showing the presence of major peaks were documented. Friability, hardness, and disintegration time of ideal batch was 0.09 ± 0.0057, 4.03 ± 0.087, and 25.57 ± 0.4860 min, respectively, and it was found to be within the set limit. Weight variation was <5%. Total fungal and bacterial counts were found to be within the limit.
Standards were established for poly herbal formulation QT, which may be used as reference for preparation and standardization of QT.
In this work Standardization of anti-diabetic tablet Qurse Tabasheer with diverse ingredients including herbal and mineral origin drugs has been attempted with identification of its ingredients, formulation, physicochemical evaluation and HPTLC finger printing, which may help in preparing consistent and better efficacious formulations. Abbreviations Used: QT: Qurse Tabasheer TLC: thin layer chromatography HPTLC: high-performance thin layer chromatography WHO: World health organization FRLHT: Foundation for Revitalization of Local Health Traditions Fe2O3: Iron oxide Sio2: Silica CaCo3: Calcium carbonate, Tio2: Titanium Oxide NIUM: National Institute of Unani Medicine #: Mesh size LOD: Loss of weight on drying USP: United state Pharmacopeia UV: Ultra Violet λ: Lambda θ: theta CFU: Colony-forming unit.
为了使尤纳尼医学更易被接受,对尤纳尼多草药配方进行质量控制是当务之急。库尔西·塔巴希尔片(QT)是一种含有六种成分的尤纳尼多草药配方,这些成分包括塔巴希尔(硅质凝结物)(簕竹)、古勒·苏尔克(大马士革蔷薇花)、古尔纳尔(石榴花)、图赫梅·卡胡(莴苣籽)、图赫梅·胡尔法(马齿苋籽)和吉利·阿尔马尼(陶土),广泛用于治疗糖尿病。本研究旨在科学评估各种理化参数,以使该配方标准化。
评估各种理化参数,包括灰分值、水分含量、浸出值、薄层色谱(TLC)和高效薄层色谱(HPTLC)、脆碎度、崩解度、均匀度和重量差异,以实现QT的标准化。
成分由专家鉴定。按照尤纳尼医学国家药典中提及的方法并加以修改来制备片剂。基于关于脆碎度、硬度和崩解度的设定参数,为理想批次的片剂建立理化标准。对QT进行了各种参数评估,如感官特性、提取物的浸出值以及压片后的HPTLC指纹图谱。
记录了干燥失重、pH值、灰分值、浸出值等参数。定性化学试验表明存在生物碱、糖苷、单宁和甾体。记录了显示主峰存在的TLC和HPTLC指纹图谱研究。理想批次的脆碎度、硬度和崩解时间分别为0.09±0.0057、4.03±0.087和25.57±0.4860分钟,且均在设定限度内。重量差异<5%。总真菌和细菌计数均在限度内。
为多草药配方QT建立了标准,可作为QT制备和标准化的参考。
在这项工作中,尝试对含有包括草药和矿物来源药物在内的多种成分的抗糖尿病片剂库尔西·塔巴希尔进行标准化,包括其成分鉴定、配方、理化评估和HPTLC指纹图谱分析,这可能有助于制备一致性更好且疗效更佳的配方。使用的缩写:QT:库尔西·塔巴希尔;TLC:薄层色谱;HPTLC:高效薄层色谱;WHO:世界卫生组织;FRLHT:地方卫生传统振兴基金会;Fe2O3:氧化铁;Sio2:二氧化硅;CaCo3:碳酸钙;Tio2:二氧化钛;NIUM:尤纳尼医学国家研究所;#:目数;LOD:干燥失重;USP:美国药典;UV:紫外光;λ:拉姆达;θ:西塔;CFU:菌落形成单位。