Lec. 9 Dr. Saad Ali Ihsan Methods Of Drug Evaluation The aim of the drug evaluation is to identify and determine the quality of the crude drug and detecting the nature of adulteration. The evaluation of crude drug is essential because, There may be biochemical variations in the drug There may be detoriation due to storage Substitution and adulteration may be present as a result of carelessness, ignorance etc The crude drugs can be identified on the basis of their morphological, histological, and chemical characters. The different techniques involved in standardization of crude drugs are Morphological and organoleptic evaluation It refers to the evaluation of drugs by color, odor, taste, size, shape and special features like texture Microscopic evaluation This method allows more detailed examination of a drug and their identification by their known histological characters. Microscope by the virtue of its property to magnify, permits minute sections under study to enlarge so that, leaf constants, stomatal index, palisade ratio can be determined. Physical evaluation These are rarely constant for crude drugs, but may help in evaluation with reference to moisture content, specific gravity, density, optic rotation, refractive index, melting point, viscosity, solubility etc. Chemical evaluation It compromises of different chemical test and assays. The isolation, purification and identification of active constituents are the methods of evaluation. Quantitative chemical test such as acid value, saponification value etc are also covered under these techniques. Biological evaluation When the estimation of potency of crude drug or its preparations are done by means of measuring its effect on living organisms like bacteria, fungal growth, or animal tissue, it is known as biological effect of the drug, compared to the standard drug. By these methods a crude drug can be assessed and further clinical trial can be recommended. Spectroscopical evaluation. (i) Ultra-violet & visible spectro photometry: Measurement of light absorption by substances in the wavelength region from 190 to 900nm.The region from 190 to 380 is known as the UV region &from 380 to 900nm,the visible region of the spectrum. Absorption in the UV-visible region arises from electronic transitions within the molecule. (ii) Infra-Red spectroscopy I.R is the study of the reflected ,absorption or transmitted radian energy in region of electromagnetic spectrum ranging from wave length ,0.8 to 500nm.I.R spectrum is divided in to three regions (a)near I.R 2500 TO 4000 cm-1 (b) mid I.R 4000 TO 400cm-1 (c) far I.R 400 to 20 cm-1 ,only the mid region is referred to simply as infra red &widely used in the analysis of drugs &pharmaceuticals. (iii) Fluorescence analysis Fluorescence means the substance in diluted acid solution. absorb light over a specific range of wavelength &re-emission of absorbed light lasts only while the substance is receiving the exciting rays .The drug belladonna leaf &root ,aloes ,jalap show fluorescence in visible range .The UV light obtained from mercury vapor lamp produce fluorescence in many natural products .e.g cinchona gives purple blue fluorescence ,wild cherry gives mauve fluorescence. (iv) Nuclear magnetic resonance spectroscopy (NMR): NMR means absorption of radiofrequency radiation by substances held in a magnetic field .NMR important tool for illustration of molecular structure, specially the stereochemistry &configuration (v) Mass spectrometry : Is concerned with the electron ionization ,subsequent fragmentation of molecules ,determination of the mass to charge ratio(m/e) & relative abundances of ions which are produced. The application of mass spectrometry is in determination of molecular weight of compounds. (vi) X-ray diffraction: Electromagnetic radiations of wave-lengths ,commonly generated by passing high voltage current(about 10,000 volts)through a Coolidge tube; they are able to penetrate most substances to some extent &to affect a photographic plate (vii) Radioimmuno assays (RIA): The assay depends on the highly specific reaction of antibodies to certain antigens. ********************************************************************************