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Review
. 2010 Sep 15;11(9):3298-322.
doi: 10.3390/ijms11093298.

Materials for pharmaceutical dosage forms: molecular pharmaceutics and controlled release drug delivery aspects

Affiliations
Review

Materials for pharmaceutical dosage forms: molecular pharmaceutics and controlled release drug delivery aspects

Heidi M Mansour et al. Int J Mol Sci. .

Abstract

Controlled release delivery is available for many routes of administration and offers many advantages (as microparticles and nanoparticles) over immediate release delivery. These advantages include reduced dosing frequency, better therapeutic control, fewer side effects, and, consequently, these dosage forms are well accepted by patients. Advances in polymer material science, particle engineering design, manufacture, and nanotechnology have led the way to the introduction of several marketed controlled release products and several more are in pre-clinical and clinical development.

Keywords: biodegradable; biomaterials; copolymers; manufacture; microparticle; nanoparticle; particle engineering design; pharmaceutical dosage forms; polymers.

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Figures

Figure 1
Figure 1
Structures of biodegradable and biocompatible polymers.
Figure 2
Figure 2
Various therapeutic agents from different therapeutic classes that have been encapsulated in polymeric particles.

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References

    1. Minko T. Drug Delivery Systems-Controlled Drug Release. In: Sinko PJ, editor. Martns Physical Pharmacy and Pharmaceutical Sciences. Lippincott Williams & Wilkins; Baltimore, MD, USA: 2006. pp. 667–672.
    1. Jantzen GM, Robinson JR. Sustained- and Controlled-Release Drug Delivery Systems. In: Banker GS, Rhodes CT, editors. Modern Pharmaceutics. Marcel Dekker, Inc; New York, NY, USA: 2002. pp. 501–528.
    1. Longer MA, Robinson JR. Sustained-Release Drug Delivery Systems. In: Gennaro AR, editor. Remington’s Pharmaceutical Sciences. Mack Publishing Company; Easton, PA, USA: 1990. pp. 1676–1693.
    1. Ebube NK, Hikal AH, Wyandt CM, Beer DC, Miller LG, Jones AB. Sustained release of acetaminophen from heterogeneous matrix tablets: Influence of polymer ratio, polymer loading, and co-active on drug release. Pharm. Dev. Technol. 1997;2:161–170. - PubMed
    1. Miyazaki Y, Yakou S, Takayama K. Study on jelly fig extract as a potential hydrophilic matrix for controlled drug delivery. Int. J. Pharm. 2004;287:39–46. - PubMed

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