Homeopathic drug standardization through biological evaluations: An untrodden avenue

There is a dearth of chemico-analytical or instrumental methods for standardization and quality control of higher dilutions of homeopathic drugs. Aim: This review highlights the challenges in standardization of anti-inflammatory homeopathic drugs and suggests a battery of biological assays for their standardization. Methods: We retrieved a total 57 scientific reports from the experimental studies and scientific reviews published between January 1999 and June 2014 related to anti-inflammatory homeopathic drugs and their high dilutions. These comprised of 18 reports on preclinical evaluation, 15 on source materials, 9 on isolated constituents and 15 studies on in-vitro experiments. Few recent citations which supported the initial studies were added later during the compilation of the manuscript. Conclusion: Standardization and quality control of homeopathic mother tinctures and high dilutions warrants an urgent attention. As biological activities are observed to be attributed to the high dilutions which are practically devoid of active ingredients, their standardization may be done through the suggested battery of biological investigations. It is suggested that the current methods of standardization of homeopathic drugs need to be upgraded to include sensitive, reproducible and relevant biological assays so that the end users are assured of the quality, efficacy, and safety of homeopathic dilutions...

Topical anti-inflammatory action of Caryocar villosum oil (Aubl) Pers.

The piquia (Caryocar villosum (Aubl.) Pers.) has drawn the attention of the scientific community for its potential as an oilseed crop species. The aim of this study was to evaluate in vivo the topical anti-inflammatory activity of fixed oil from Caryocar villosum (Aubl.) Pers. – OCV. To evaluate anti-inflammatory activity, the following assays were used in rats: a) granuloma assay (cotton-pellet), b) carrageenan-induced paw edema and c) vascular permeability assay. Gas chromatography analysis from the OCV, transesterified with a BF3-methanol sample, showed the following fatty acid esters to be major compounds of this species: methyl hexadecanoate (32%), methyl octadecanoate (29%) and methyl (E)-octadecanoate (29%). The ED50 calculated from the granuloma assay was 531 mg/kg. In the granuloma assay, rat model of carrageenan-induced paw edema and vascular permeability of histamine test, groups treated with a topical dose of 531 mg/kg OCV showed significant differences (p < 0.05, analysis of variance (ANOVA) followed by a multiple comparison Student-Newman-Keuls test) when compared to the control groups treated with distilled water. Thus, a 531 mg/kg dose of OCV elicited a topical anti-inflammatory effect in rats, and the fatty acid esters identified in the fixed oil from Caryocar villosum participate in the detected topical anti-inflammatory activity because compounds with this characteristic are capable of modulating acute and chronic inflammatory responses.

Correlation evaluation of transdermal delivery in vitro and in vivo with Zhibitong Cataplasm / 中草药

Objective: To investigate the correlation of transdermal delivery in vitro and in vivo with Zhibitong Cataplasm. Methods: Single-chamber diffusion cell was used and sinomenine concentration was determined by HPLC in vitro. In vivo tests, W-N method was applied to calculating the cumulative absorption of concentration by plasma drug concentration in rats. And the linear regression equation was figured through the concentration of cumulative in vitro and the concentration of cumulative absorption in vivo. Results: The regression equation was Y=0.097 24 X+0.323 91, r=0.955 1 and there was a high correlation between in vitro transdermal delivery and in vivo percutaneous absorption. Conclusion: This method can be used to evaluate the correlation between in vitro and in vivo transdermal delivery.