Parameters affecting in-liquid drying microencapsulation and release rate of cefaclor

Author:

Chow Albert H.L.,Ho Susan S.S.,Tong Henry H.Y.,Ma Henry H.M.

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference6 articles.

1. Harvey, S.C., 1990. Antimicrobial drugs. In: Gennaro, A.R., Chase, G.D., Marderosian, A.D., Harvey, S., Hussar, D.A., Medwick, T., Rippie, E., Schwartz, J.B., Swinyard, E.A., Zink, G.L. (Eds.), Remington's Pharmaceutical Sciences, 18th ed. Mack, Easton PA, pp. 1163–1241.

2. Mechanism of sustained-action medication: theoretical analysis of rate of release of solid drugs dispersed in solid matrices;Higuchi;J. Pharm. Sci.,1963

3. Huls, C.E., Mullenix, T.A., Prince, R.A., 1992. Upper respiratory tract infections. In: Herfindal, E.T., Gourley, D.R. and Hart, L.L. (Eds.), Clinical Pharmacy and Therapeutics, 5th ed. Williams and Wilkins, Baltimore MD, pp. 1062–1079.

4. Lorenz, L.J., 1980. Cefaclor. In: Florey, K. (Ed.), Analytical Profiles of Drug Substances, vol. 9. Academic Press, New York, pp. 107–123.

5. Thies, C., 1992. Formation of degradable drug-loaded microparticles by in-liquid drying processes. In: Donbrow, M. (Ed.), Microcapsules and Nanoparticles in Medicine and Pharmacy. CRC Press, Boca Raton, FL, pp. 47–71.

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