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Formulation characterization

Antiwear premium hydrauHc fluids represent the largest volume of hydrauHc fluids used. Shortly after their introduction in 1960, a second product group was formulated, characterized by the same antiwear characteristics but having lower pour points and higher viscosity indexes. These were formulated for use in mobile and marine appHcations subject to temperature extremes. [Pg.262]

Nayak B, Panda AK, Ray P et al (2009) Formulation, characterization and evaluation of rotavirus encapsulated PLA and PLGA particles for oral vaccination. J Microencapsul 26 154-165... [Pg.64]

Formulation Characterization. Prior to using a new propellant formulation in pilot-plant or production studies, the material must be fully characterized and analyzed Theologically. Processability predictions may be extrapolated from this step. [Pg.178]

Shire, S. J. (1996), Stability, characterization and formulation of recombinant human deoxyribonuclease (Pulmozyme , Dornase Alpha), in Pearlman, R., and Wang, Y. J. Eds., Formulation, Characterization and Stability of Protein Drugs, Plenum Press, New York, pp. 393 126. [Pg.685]

Element Hardness in units of 10-degree Mohs scale measured at 293 K Theoretical j hardness j calculated j Additional from formulal characterization of sample W1 ) = a- r/ y Measure- ment tempera- ture K Measured hardness ... [Pg.150]

Radomska-Soukharev, A. and R. H. Mueller. 2006. Chemical stability of lipid excipients in SLN-production of test formulations, characterization and short-term stabflH armazid51 425-430. [Pg.304]

Herman AC, Boone TC, Lu HS. Characterization, formulation, and stability of Neupogen (filgrastim), a recombinant human granulocyte-colony stimulating factor. In Pearlman R.WangYJ (Eds.), Formulation, Characterization, and Stability of Protein Drugs. New York, NY Plenum Press 1996 303-328. [Pg.391]

Volkin, D. B., and Middaugh, C. R. (1996). The characterization, stabilization, and formulation of acidic fibroblast growth factor. In Formulation, characterization, and stability of protein drugs (R. Pearlman and Y. J. Wang, eds.), pp. 181-217. Plenum, New York. [Pg.70]

Reddy, L. H., Sharma, R. K., Chuttani, K., Mishra, A. K., and Murthy, R. R. (2004), Etoposide-incorporated tripalmitin nanoparticles with different surface charge Formulation, characterization, radiolabeling, and biodistribution studies, AAPS J., 6(3), e23. [Pg.562]

Powell, M.F. A Compendium and hydropathy/flexibility analysis of common reactive sites in proteins reactivity at Asn, Asp, Gin, and Met Motifs in neutral pH solution. In Formulation, Characterization, and Stability of Protein Drugs Pearlman, R., Wang, Y.J., Eds. Plenum Press New York, NY, 1996 1-140. [Pg.298]

Preparation by Skraup synthesis from 2,4-dinitroaniline and glycerol, followed by treatment with ethanol. The reagent is a specific precipitant for hydroperoxides. Thus Rieche et al., on achieving the synthesis of allylhydroperoxide in preparative quantity by the method formulated, characterized the compound by conversion into the derivative (2), which forms yellow needles, m.p. 101. 5-103°. [Pg.914]

Interesting case histories about formulation, characterization and stability of protein drugs are discussed in the book edited by Pearlman and Wang. ... [Pg.845]

See Powell, M.F., in Formulation, Characterization, and Stability of Protein Drugs, Plenum Press, New York, 1996, pp. 1—140. [Pg.445]

Albert H.L. Chow, School of Pharmacy, The Chinese University of Hong Kong, Shatin, NX, Hong Kong, China, Stability Assessment and Formulation Characterization... [Pg.1673]


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See also in sourсe #XX -- [ Pg.53 ]




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