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Pharmaceutical Coating Technology (Part 11)

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This chapter will highlight all the activities that are necessary to ensure that all aspects of the coating process are fully documented from design through to operation, to provide compliance with regulatory requirements.. 11.1 INTRODUCTION. Among the most relevant of the regulatory issues from the Code of Federal Regulations, Volume 21, that should be considered in the assembly of any...

Pharmaceutical Coating Technology (Part 12)

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One of the requirements of a film coat is that it should provide adequate protection to the dosage form. The capacity of the film coat to afford physical protection depends to a large extent on its mechanical characteristics. One of the requirements of a film coat is that it should provide adequate physical protection to the dosage form. The capacity...

Pharmaceutical Coating Technology (Part 13)

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This was attributed to the increase in the roughness of the coat. Because of the difficulties in achieving glossy film. 13.1 Diagrammatic representation of the calculation of arithmetic mean roughness.. Page 365 atomized film-coating droplets on the substrate surface and thus aid the optimization of the coating process. Coat surface roughness will be dependent upon the roughness of the substrate,...

Pharmaceutical Coating Technology (Part 14)

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Relevant aspects of the composition and performance of modified release coatings are considered in this chapter. The properties and effects of the polymers and plasticizers which are used in modified release coatings are illustrated with examples from the literature. The following factors as they affect enteric performance are described in some detail: the enteric polymer, the film formulation, the stability...

Pharmaceutical Coating Technology (Part 15)

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Question: What major process and formulation parameters do I need to take into account in the change from organic solvent coating to aqueous coating?. Answer: Looking first of all at the formulation-based parameters, there is a need to increase the solids loading of the coating suspension to something like 12 %w/w if using a typical. Maximizing solids will usefully minimize...

Pharmaceutical Coating Technology (Part 16)

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A PHARMACEUTICAL FILM COATING PUBLICATIONS BIBLIOGRAPHY This chapter contains a comprehensive listing of research papers, reviews, book chapters and theses covering the subject of pharmaceutical film coating. Film-coating materials (polymers, additives, formulation—including solutions and suspension properties). Physicochemical properties of coating systems (including interactions of polymers and additives, and thermomechanical properties). (1966) Film coating theory and practice. (1978) Aqueous cellulosic film...

HPLC for Pharmaceutical Scientists 2007 (Part 7A)

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Rapid development of MS in recent decades has further expanded its role in the structural characterization of small molecules in the drug discovery process [1].. In combination with chromatographic separation techniques, principally in the form of high-performance liquid chromatography (HPLC. In addition, control of internal energy deposited on ions during ionization should be achievable in the ionization source to control...

HPLC for Pharmaceutical Scientists 2007 (Part 7B)

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The characteristic isotopic patterns resulting from combi- nations of the isotope peaks can be used to ascertain elemental composition of the corresponding ion.. In the case of Verapamil (Scheme 1), the molecular weight of the com- pound is 420 Da, indicating an even number of nitrogen atoms in the molecule.. The change of chromatographic retention time due to the use...

HPLC for Pharmaceutical Scientists 2007 (Part 8A)

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The aim of analysis of each HPLC method may vary for each developmental area in the drug development process and specific examples are given in Section 8.2.. These include properties of the analyte, detector, mobile phase, stationary phase, and gradient considerations.. The final part of the chapter provides a refresher on “pK a from an analy- tical chemist’s perspective,” the...

HPLC for Pharmaceutical Scientists 2007 (Part 8B)

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Also the spectral homogeneity of the peak of interest must be taken into consideration. If the peak is not spectrally homogenous, the overlay of the spectra will show. This does not absolutely ascertain that the peak is homogeneous since isomers of the same compound will have the same [M + H] and is indistin- guishable from the parent compound. and...

HPLC for Pharmaceutical Scientists 2007 (Part 8C)

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If the retention of the early eluting components are consistent (less than 1% variation in reten- tion time) in all three methods, then the lowest equilibration time could be used. Optimization of the optimal equilibration time is required for reproducible methods.. The dwell volume should be determined for all the systems in the laboratory and based on these determinations, this...

HPLC for Pharmaceutical Scientists 2007 (Part 8D)

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Extreme changes in selectivity and reversal of elution order of phenolic isomeric compounds were obtained after changing either the pH of the mobile phase, the temperature of the system, or the type of organic eluent employed. Changes in the analyte ion- ization state were observed upon increasing the acetonitrile composition as well as the temperature. Method development for ionizable analytes...

HPLC for Pharmaceutical Scientists 2007 (Part 8E)

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Therefore to enhance the retention of this potential degradation product the initial organic composition of the gradient was reduced from 35%. ion of the impurity that has been resolved from the main peak. The mass spectrum of the impurity (RRT 1.04) that has now been resolved from the main peak was also taken. MS conditions flow split 10 : 1....

HPLC for Pharmaceutical Scientists 2007 (Part 8F)

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The extent to which an organic molecule absorbs electromagnetic radiation in the ultraviolet region (UV light) depends on the structure of the molecule.. The pH of the mobile-phase effects the ionization of ionogenic solutes and also the analyte UV response. The change in pH can change the electronic structure of the molecule and result in changes in the molar absorptivity...

HPLC for Pharmaceutical Scientists 2007 (Part 1)

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This lead to the final selection of the most potentially viable therapeutic candidates that are taken forward to drug development. Chromatographic separations are based on a forced transport of the liquid (mobile phase) carrying the analyte mixture through the porous media and the differences in the interactions at analytes with the surface of this porous media resulting in different migration...

HPLC for Pharmaceutical Scientists 2007 (Part 2)

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Dynamic transfer of the analyte molecules between mobile phase and adsorbent surface in the presence of secondary equilibria effects is also only part of the processes responsible for the analyte retention on the column. Efficiency is the measure of the degree of peak dispersion in a particular column. as such, it is essentially the characteristic of the column. If H...

HPLC for Pharmaceutical Scientists 2007 (Part 3)

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Due to the exponential nature of the rela- tionship between retention and interaction energy even the presence of 1%. Bonding density is the primary parameter in evaluation of the quality of the bonded material. All parameters of the packing material are interrelated in their influence on the chromatographic performance of the column. Macropores in the monolith are between 4000 and...

HPLC for Pharmaceutical Scientists 2007 (Part 4A)

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At the same time, the pHs of aqueous–organic mixtures are different from the pH of the aqueous compo- nent itself. The basis for the analyte retention in reversed-phase chromatography is the competitive interactions of the analyte and eluent components with the adsor- bent surface. The stronger the interactions of the analyte with the surface, the longer its retention. Selectivity or...

HPLC for Pharmaceutical Scientists 2007 (Part 4B)

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An empirical formula representing the variation of the δ quantity with mole fraction of acetonitrile (χ) from the values in Table 4-4 could be determined using equation (4-20). It was shown that the s s pH of the eluent increases with an increase of acetonitrile content. The change in the mobile-phase pH of a particular buffer as a function of...

HPLC for Pharmaceutical Scientists 2007 (Part 4C)

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Figure 4-45 shows the similar retention dependencies of adrenaline retention for different amphiphilic ions adsorbed on the surface of the reversed-phase material, indi- cating that at the same surface concentration of any amphiphilic ion adsorbed, the retention of basic analyte is the same. Comparison of Figures 4-46 and 4-45 indicates that the retention of a charged analyte in ion-pairing mode...