两种不同培养基制备罗沙曼加的比较药学分析研究

Ayu Pub Date : 2020-07-01 DOI:10.4103/ayu.AYU_261_19
Dipali Parekh, Sarika M. Makwana, P. Bedarkar, B. Patgiri
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引用次数: 1

摘要

引言:首先,Rasamanikya是由Acharya Dhundhuknath在Rasendra Chintamani中描述的。它是一种由含砷药物,即orpiment (Haratala)制备的制剂。Haratala在Rasa经典中被归类为Uparasa Varga,也被列入1940年D和C法案的附表E1。在经典中,有很多媒体提到了净化过程(Shodhana)的装饰。在本研究中,Kushmanda Swarasa (Benincasa hispida [Thunb]的汁液)。[cn] Cogn)和Churnodaka(石灰水)作为净化介质。目的:本研究的目的是规范沙散散的制药工艺,并对库什曼达·斯瓦拉萨和原塔拉斯达制备的沙散散进行比较分析。材料与方法:本研究分两阶段进行,分别为:原达拉散食法和Kupipakwa法制备罗刹散食法。对两种药材的感官和理化参数进行了分析。通过x射线衍射(XRD)、电感耦合等离子体-原子发射光谱(ICP-AES)、CHNS和O、场发射枪扫描电子显微镜(fg - sem)、傅里叶变换红外光谱(FTIR)和热重分析(TGA)等精密分析参数对最终产品样品进行了分析。结果:以纯化的黄芪600 g为原料,平均制备时间为2 h。在XRD分析中,两种样品具有不同的衍射模式。在ICP-AES分析中,两种样品的砷含量相同。用Churnodaka Shodhita Haratala制备的Rasamanikya的TGA损失百分比大于Kushmanda Swarasa Shodhita Haratala。结论:两种不同培养基制备的罗沙曼加在制药工艺上无明显差异。然而,在分析研究中存在相当大的差异。Kupipakwa法可用于大规模制备。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative pharmaceutico-analytical study of Rasamanikya prepared by two different Shodhana media of Haratala (orpiment)
Introduction: Foremost, Rasamanikya is described in Rasendra Chintamani by Acharya Dhundhuknath. It is a formulation that is prepared from the arsenical drug, i.e., orpiment (Haratala). Haratala is classified under Uparasa Varga in Rasa classics and is also included under Schedule E1 in D and C act 1940. In classics, there are so many media mentioned for purification process (Shodhana) of orpiment. In the present study, Kushmanda Swarasa (juice of Benincasa hispida [Thunb.] Cogn) and Churnodaka (lime water) are adopted as the purification media for orpiment. Aim: The aim of this study was to standardize the pharmaceutical procedure of Rasamanikya and develop a comparative analytical profile of both the formulation, i.e., Rasamanikya prepared by Kushmanda Swarasa and Churnodaka Shodhita Haratala. Materials and methods: The study was carried out in two stages as follows: Shodhana of Haratala and preparation of Rasamanikya by Kupipakwa method. Both the samples of Rasamanikya were analyzed for organoleptic and physicochemical parameters. The samples of final products were also analyzed through sophisticated analytical parameters, i.e., X-ray diffraction (XRD), Inductively coupled plasma-atomic emission spectroscopy (ICP-AES), CHNS and O, Field emission gun-scanning electron microscopy (FEG-SEM), Fourier transform infrared spectroscopy (FTIR) and Thermo-gravimetric analysis (TGA). Results: Average 2 h duration was required for the preparation of Rasamanikya formulation from 600 g of purified orpiment. In XRD analysis, both samples have different diffraction patterns. In ICP-AES analysis, both samples have the same percentage of arsenic. More percentage loss was noted in the TGA of Rasamanikya prepared with Churnodaka Shodhita Haratala than that of Kushmanda Swarasa Shodhita Haratala. Conclusion: Rasamanikya prepared by two different media of Shodhita Haratala did not found to have a substantial difference in pharmaceutical procedure. However, there was a considerable difference in the analytical study. Kupipakwa procedure can be used for large-scale preparation.
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Ayu
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