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unit i pharmaceutical analysis definition and scope 1 pharmaceutical analysis pharmaceutical analysis may be defined as the application of analytical procedures used to determine the purity safety and quality of ...

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           Unit I Pharmaceutical Analysis Definition and Scope                                       !1.
           Pharmaceutical Analysis :  
             
                Pharmaceutical analysis may be defined as the 
           application  of  analytical  procedures  used  to 
           determine the purity, safety and quality of drugs 
           and  chemicals.  The  term  "Pharmaceutical 
           Analysis"  is  otherwise  called  Quantitative 
           pharmaceutical chemistry. Pharmaceutical analysis 
           includes both qualitative and quantitative analysis 
           of  Drugs  and  Pharmaceutical  substances  starts 
           from bulk drugs (starting material) to the finished 
           dosage forms. In modern practice of medicine, the 
           analytical  methods  are  used  in  the  analysis  of 
           chemical  constituents  found  in  the  human  body 
           whose altered concentrations during disease states 
           serve as diagnostic aids and also used to analyse the medicinal agents and their metabolites found in 
           biological system. 
                 Pharmaceutical analysis is a branch of practical chemistry that involves a series of process for 
           identification,  determination,  quantification  and  purification  of  a  substance,  separation  of  the 
           components of a solution or mixture, or determination of structure of chemical compounds.The 
           substance may be a single compound or a mixture of compounds and it may be in any of the dosage 
           form. The substance used as pharmaceuticals are animals, plants, micro organisms, minerals and 
           various synthetic products. 
           The sample to be analysed is called as analyte and on the basis of size of sample, they can be 
           classified as macro(0.1 g or more), semi micro (0.01 g to 0.1 g), micro(0.001 g to 0.01 g), sub micro 
           (0.0001 g to 0.001 g), ultramicro (below 10-4 g), trace analysis(100 to 10000 ppm). Among all, the 
           semi micro analysis is widely used. 
                In modern practice of pharmacy it is important that Pharmacists have more than an appreciation 
           of quantitative analytical methodology. The term Quality as applied to a drug product has been 
           defined as the sum of all factors which contribute directly or indirectly to the safety, effectiveness 
           and reliability of the product. These properties are built into drug products through research and 
           during the manufacturing process by procedures collectively referred to as "Quality Control". 
           Quality control guarantees within reasonable limits that a drug product : 
           1. Is free from impurities 
           2. Is physically and chemically stable 
           3. contains the amount of active ingredient(s) as stated on the label 
           4. provides optimal release of active ingredient(s) when the product is administered. 
           TYPES OF ANALYSIS 
           There are main two types of chemical analysis. 
           1. Qualitative (identification) 
           2. Quantitative (estimation) 
           1. Qualitative analysis is performed to establish composition of natural/synthetic substances. 
           These tests are performed to indicate whether the substance or compound is present in the sample 
           Unit I Pharmaceutical Analysis Definition and Scope                                        !2.
           or not. Various qualitative tests are detection of evolved gas, formation of precipitates, limit tests, 
           colour change reactions, melting point and boiling point test etc.
           2. Quantitative analytical techniques are mainly used to quantify any compound or substance in 
           the sample. These techniques are based in (a) the quantitative performance of suitable chemical 
           reaction and either measuring the amount of reagent added to complete the reaction or measuring 
           the amount of reaction product obtained, (b) the characteristic movement of a substance through a 
           defined medium under controlled conditions, (c) electrical measurement, (d) measurement of some 
           spectroscopic properties of the compound.
           SCOPE OF PHARMACEUTICAL ANALYSIS
           1.Chemical methods 
           a)Titrimetric or volumetric method
           It involves reaction of substance to be determined with an appropriate reagent as a standard 
           solution, and volume of solution required to complete the reaction is determined. Volumetric 
           methods require simple and less apparatus and they are susceptible of high accuracy.
           Various types of titrimetric methods are:
           i)Acid-base titrations (neutralization reactions)
           ii)Complexometric titrations
           iii)Precipitation titrations
           iv)Oxidation reduction titrations
           v)Non aqueous titrations
           b)Gravimetric methods
           In gravimetric analysis, a substance to be determined is converted into an insoluble precipitate in 
           the purest form, which is then collected and weighed. It is the time consuming process.
           In electrogravimetry, electrolysis of the sample is carried out on the electrodes is weighed after 
           drying.
           Thermogravimetry (TG) records the change in weight, differential thermal analysis (DTA) records 
           the difference in temperature between test substance and an inert reference material, differential 
           scanning calorimetry (DSC) records the energy needed to establish a zero temperature difference 
           between a test substance and reference material.
           c)Gasometric analysis
           Gasometry involves measurement of the volume of gas evolved or absorbed in a chemical reaction.
           Some of the gases which are analysed by Gasometry are CO  , N O, cyclopropane, amyl nitrate, 
           ethylene, N , helium etc.                                  2   2
                      2
           2.Electrical methods
           Electrical methods of analysis involve the measurement of electric current, voltage or resistance in 
           relation to the concentration of some species in the solution.
           Electrical methods of analysis include:
           (a)Potentiometry
           (b)Conductometry
           (c)Polarography
           (d)Voltametry
           (e)Amperometry
           Potentiometry measures electrical potential of an electrode in equilibrium with an ion to be 
           determined. Conductometry measures electrical conductivity of an electrode with a reference 
           Unit I Pharmaceutical Analysis Definition and Scope                                       !3.
           electrode while Polarography, Voltametry and Amperometry measures electrical current at a 
           micro-electrode.
           3.Instrumental methods of analysis
           Instrumental method involves measurement of some physical properties of the compound or a 
           substance. These methods are employed for determination of minor or trace concentration of 
           element in the sample.
           Instrumental methods are preferred due to their selectivity, high speed, accuracy and simplicity of 
           analysis. Any change in the properties of the system are detected by measurement of absorbance, 
           specific rotation, refractive index, migration difference, charge to mass ratio etc.
           Spectroscopic methods of analysis depend upon measurement of the amount of radiant energy of a 
           particular wavelength emitted by the sample.
           Methods which include absorption of radiation are ultra violet, visible, infra red, atomic 
           absorption, nuclear magnetic resonance spectroscopy etc.
           Emission methods involve heating or electrical treatment of the sample so that the atoms are raised 
           to the excited state to emit the energy and the intensity of this energy is measured. Emission 
           methods include emission spectroscopy, flame photometry, flourimetry etc.
           Chromatographic techniques and electrophoretic methods are separation methods for the mixture 
           of   compounds,   but   also   applied   for   identification   of   compounds   of   mixtures.   Various 
           chromatographic techniques are GC, HPLC, TLC, HPTLC, PC etc.
           Mass spectrometry involves vaporisation of material using a high vacuum and the vapour is 
           bombarded by a high energy electron beam. Vapour molecules undergo fragmentation to produce 
           ions of varying size. These ions are differentiated by accelerating them in electrical field and then 
           deflecting them in a magnetic field. Each kind of ion gives a peak in the mass spectrum.
           4.Biological and microbiological methods
           Biological methods are used when potency of a drug or its derivative can not be properly 
           determined by any physical or chemical methods. They are called bio-assays.
           Microbiological methods are used to observe potency of antibiotic or anti- microbial agents. In 
           antimicrobial assay, inhibition of growth of bacteria of the sample is compared with that of the 
           standard antibiotic. These methods include cup plate method and turbidimetric analysis.
           APPLICATIONS
           Manufacturing industries require both qualitative and quantitative analysis to ensure that their 
           raw materials meet certain specifications, and to check the quality of final product. Raw materials 
           are to be checked to ensure that the essential components are present within the predetermined 
           range of composition and there are not any unusual substances present which might upset the 
           manufacturing process or it may appear as a harmful impurity in the final product.
           In the development of new products which contains mixtures other then the pure material, it is 
           necessary to ascertain composition of mixture which shows the optimum characteristics for which 
           the material has been developed.
           Geographical surveys require analysis to determine the composition of soil sample and numerous 
           rock samples collected from the field.
           Most of the industrial processes give rise to pollutants which may cause health related problems. 
           So quantitative analysis of air, water and soil sample should be carried out to determine the level 
           of pollution and to establish the safe limits for pollutants.
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...Unit i pharmaceutical analysis definition and scope may be defined as the application of analytical procedures used to determine purity safety quality drugs chemicals term is otherwise called quantitative chemistry includes both qualitative substances starts from bulk starting material finished dosage forms in modern practice medicine methods are chemical constituents found human body whose altered concentrations during disease states serve diagnostic aids also analyse medicinal agents their metabolites biological system a branch practical that involves series process for identification determination quantification purification substance separation components solution or mixture structure compounds single compound it any form pharmaceuticals animals plants micro organisms minerals various synthetic products sample analysed analyte on basis size they can classified macro g more semi sub ultramicro below trace ppm among all widely pharmacy important pharmacists have than an appreciation ...

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