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International Journal of Pharmaceutics

Trommer, H. Neubert, R.H. (2005). The examination of polysaccharides as potential antioxidative compounds for topical administration using a lipid model system. International Journal of Pharmaceutics, Vol. 298, No. 1, 0uly 2005), pp.153-163, ISSN 0378-5173. [Pg.25]

Andry, M. C., Edwards-Levy, F. Levy, M. C. (1996). Free amino group content of serum albumin microcapsules. III. A study at low pH values. International Journal of Pharmaceutics, Vol. 128,1-2, (February 1996), pp. (197-202), ISSN 0378-5173... [Pg.79]

Raffin, R. P., Jornada, D. S., Re, M. L, Pohimann, A. R. Guterres, S. S. (2006). Sodium pantoprazole-loaded enteric microparticles prepared by spray drying Effect of the scale of production and process validation. International Journal of Pharmaceutics, Vol. 324,1, (October 2006), pp. (10-18), ISSN 0378-5173... [Pg.82]

Ribeiro, A. J., Neufeld, R. Arnaud, P. Chaumeil, J. C. (1999). Microencapsulation of lipophilic drugs in chitosan-coated alginate microspheres. International Journal of Pharmaceutics, Vol. 187,1, (September 1999), pp. (115-123), ISSN 0378-5173 Rubinstein, A. (1995). Approaches and opportunities in colon-specific drug-delivery. Critical Reviews in Therapeutic Drug Carrier Systems, Vol 12, 2-3,1995), pp. (101-149), ISSN 0743-4863... [Pg.83]

Zeevi, A., Klang, S., Alard, V., Brossard, F. and Benita, S. (1994) The design and characterization of a positively charged submicron emulsion containing a sunscreen agent. International Journal of Pharmaceutics, 108 (1), 57-58. [Pg.170]

Bouchemal, K., Briangon, S., Perrier, E. and Fessi, H. (2004) Nano-emulsion formulation using spontaneous emulsification solvent, oil and surfactant optimisation. International Journal of Pharmaceutics, 280, 241-251. [Pg.171]

Klang, V., Matsko, N., Zimmermann, A.M., Vojnikovic, E. and Valenta, C. (2010) Enhancement of stability and skin permeation by sucrose stearate and cydodextrins in progesterone nanoemulsions. International Journal of Pharmaceutics, 393, 152—160. [Pg.171]

Perrier, T., Saulnier, P., Fouchet, F., Lautram, N. and Benoit, J.P. (2010) Postinsertion into Lipid NanoCapsules (LNCs) from experimental aspects to mechanisms. International Journal of Pharmaceutics, 396, 204—209. [Pg.172]

Martin, G.P. and Nokhodchi, A. (2006) The microsponge delivery system of benzoyl peroxide preparation, characterization and release studies. International Journal of Pharmaceutics, 308, 124-132. [Pg.173]

Allemann, E., Gurny, R. and Doelker, E. (1992) Preparation of aqueous polymeric nanodispersions by a reversible salting-out process influence of process parameters on particle size. International Journal of Pharmaceutics, 87, 247-253. [Pg.173]

Ozyazici, M., Sevgi, F. and Ertan, G. (1996) Micromeritic studies on nicardipine hydrochloride microcapsules. International Journal of Pharmaceutics, 138, 25-35. [Pg.173]

Benita, S. and Donbrow, M. (1982) Dissolution rate control of the release kinetics of water-soluble compounds from ethylcellulose film-type microcapsules. International Journal of Pharmaceutics, 12, 251-264. [Pg.173]

Tirkkonen, S. and Paronen, P. (1992) Enhancement of drug release from ethylcellulose microcapsules using solid sodium chloride in the wall. International Journal of Pharmaceutics, 88, 39-51. [Pg.173]

Morales, M.E., Ruiz, M.A., Oliva, I., Oliva, M. and Gallardo, V. (2007) Chemical characterization with XP S of the surface of polymer microparticles loaded with morphine. International Journal of Pharmaceutics, 333, 162—166. [Pg.174]

Levis, S. and Deasy, P. (2002) Characterization of halloysite for use as a microtubular drug delivery system. Internal Journal of Pharmaceutics, 243, 125-134. [Pg.440]

Kelly, H., Deasy, P., Ziaka, E. and Claffey, N. (2004) Formulation and preliminary in vivo dog studies of a novel drug delivery system for the treatment of periodontitis. Internal Journal of Pharmaceutics, 274, 167—183. [Pg.440]

Sharma, A., and Sharma, U.S., Liposomes in drug delivery progress and limitations, International Journal of Pharmaceutics, 1997, 154, 123-140. [Pg.14]

Cortesi, R., Esposito, E., Menegatti, E., Gambari, R., Nastruzzi, C., Gelatine micro-spheres as a new approach for controlled delivery of synthetic oligonucleotides and PCR-generated fragments, International Journal of Pharmaceutics, 1994, 105, 181-186. [Pg.16]

Heydenreich, A.V., Westmeier, R., Pedersen, N., Poulsen, H.S., and Kristensen, H.G., Preparation and purification of cationic solid lipid nanospheres effects on particle size, physical stability and cell toxicity, International Journal of Pharmaceutics, 2003, 254, 83-87. [Pg.17]

Wang, W. 2000. Lyophilizatin and development of solid protein pharmaceuticals. International Journal of Pharmaceutics 203(1-2), 1-60. [Pg.172]

Wei, W. 1999. Instability, stabilization and formulation of liquid protein pharmaceuticals. International Journal of Pharmaceutics 185(2), 129-188. [Pg.172]

Hillery, A.M. and A.T. Florence, The Effect of Adsorbed Poloxamer 188 and 407 Surfactants on the Intestinal Uptake of 60-nm Polystyrene Particles after Oral Administration in the Rat, International Journal of Pharmaceutics. 132, 123, 1996. [Pg.12]

Raghuvanshi, R.S. et al., Improved Immune Response from Biodegradable Polymer Particles Entrapping Tetanus Toxoid by Use of Different Immunization Protocol and Adjuvants, International Journal of Pharmaceutics. 245, 109, 2002. [Pg.13]

Pikal, M. J., Shah, S. The collaps temperature in freeze-drying Dependence on measurement methodology and rate of water removal from the glassy phase. International Journal of Pharmaceutics 62, p. 165-186, 1990... [Pg.122]

Schellenz, G., Engel, J. Rupprecht, H. Sublimation during lyophilization detected by temperature profile and X-ray technique. International Journal of Pharmaceutics 113, p. 133— 140, 1995. Copyright 1995 Elsevier Science B. V. [Pg.126]

Grunenberg, A., Flenck, J-O., Siesler, FI.W., 1996, Theoretical Derivation and practical Application of Energy / Temperature Diagrams as an Instmment in Preformulation Studies of Polymorphic Drug Substances, International Journal of Pharmaceutics, 129, 147-158. [Pg.81]

Bibby DC, Talmadge JE, Dalai MK, Kurz SG, Chytil KM, Barry SE, Shand DG, Steiert M (2005) Pharmacokinetics and biodistribution of RGD-targeted doxorubicin-loaded nanoparticles in tumor-bearing mice. International Journal of Pharmaceutics 293 281-290. [Pg.258]

Rajalahti T. Kvalheim O.M. Multivariate data analysis in pharmaceutics A tutorial review. International Journal of Pharmaceutics. 2011,417 (1-2), 280-290. [Pg.71]

Loyd V. Allen, Jr., Ph.D. Editor-in-Chief, International Journal of Pharmaceutical Compounding, Edmond, Oklahoma Compounding, Contemporary... [Pg.310]

Sugano, K., Takata, N., Machida, M., Saitoh, K. and Terada, K. (2002) Prediction of passive intestinal absorption using bio-mimetic artificial membrane permeation assay and the paracellular pathway model. International Journal of Pharmaceutics, 241, 241-251. [Pg.67]

Abraham, M.H. and Acree, W.E. Jr. (2005) Characterisation of the water-isopropyl myristate system. International Journal of Pharmaceutics, 294, 121-128. [Pg.111]

Benet, L.Z., Cummins, C.L. and Wu, C.Y. (2004) Unmasking the dynamic interplay between efflux transporters and metabolic enzymes. International Journal of Pharmaceutics, 277, 3-9. [Pg.137]

Wang, Q., Rager, J.D., Weinstein, K., Kardos, P.S., Dobson, G.L., Li, J. and Hidalgo, l.J. (2005) Evaluation of the MDR-MDCK cell line as a permeability screen for the blood-brain barrier. International Journal of Pharmaceutics, 288, 349-359. [Pg.138]

Carrara, S., Reali, V., Misiano, P., Dondio, G. and Bigogno, C. (2007) Evaluation of in vitro brain penetration Optimized PAMPA and MDCKII-MDRl assay comparison. International Journal of Pharmaceutics, 345, 125-133. [Pg.138]

Sugano, K., Nabuchi, Y, Machida, M. and Asoh, Y. (2004) Permeation characteristics of a hydrophilic basic compound across a bio-mimetic artificial membrane. International Journal of Pharmaceutics, 275, 271—278. [Pg.139]

Loftsson, T., Korrradsdottir, P. and Masson, M. (2006) Development and evaluation of an artificial membrane for determination of drug availability. International Journal of Pharmaceutics, 326, 60-68. [Pg.140]


See other pages where International Journal of Pharmaceutics is mentioned: [Pg.83]    [Pg.173]    [Pg.268]    [Pg.440]    [Pg.123]    [Pg.270]   
See also in sourсe #XX -- [ Pg.848 ]




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