Literature DB >> 20230305

Techniques for efficient entrapment of pharmaceuticals in biodegradable solid micro/nanoparticles.

Tsutomu Ishihara1, Tohru Mizushima.   

Abstract

IMPORTANCE OF THE FIELD: Biodegradable solid particles are potential carriers for both hydrophobic and hydrophilic drugs and have been marketed for prolongation of pharmaceutical activity. In developing such particles, it is important to achieve stable encapsulation of the drugs in the particles and a controlled rate of drug release. AREAS COVERED IN THIS REVIEW: In this paper, the principles and techniques for preparing such particles are reviewed. WHAT THE READER WILL GAIN: Overall, it remains difficult to identify a general approach for achieving effective entrapment and controlled release, because these qualities are determined by multiple complex factors. The encapsulation efficiency of drugs in particles can be improved through various techniques, including hydrophobic interaction, covalent bonding, ionic interaction and physical isolation. In addition, the release behaviors of drugs are strongly influenced by environmental conditions as well as the physicochemical properties of the polymers and drugs. TAKE HOME MESSAGE: Solid particles with targeting ability in addition to prolongation of biological activity may have potential for development of a new type of pharmaceutical in the clinical field.

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Year:  2010        PMID: 20230305     DOI: 10.1517/17425241003713486

Source DB:  PubMed          Journal:  Expert Opin Drug Deliv        ISSN: 1742-5247            Impact factor:   6.648


  4 in total

1.  Improved drug loading and antibacterial activity of minocycline-loaded PLGA nanoparticles prepared by solid/oil/water ion pairing method.

Authors:  Tahereh Sadat Jafarzadeh Kashi; Solmaz Eskandarion; Mehdi Esfandyari-Manesh; Seyyed Mahmoud Amin Marashi; Nasrin Samadi; Seyyed Mostafa Fatemi; Fatemeh Atyabi; Saeed Eshraghi; Rassoul Dinarvand
Journal:  Int J Nanomedicine       Date:  2012-01-10

2.  Inhibitory effect of a new orally active cedrol-loaded nanostructured lipid carrier on compound 48/80-induced mast cell degranulation and anaphylactic shock in mice.

Authors:  Shreyasi Chakraborty; Nabanita Kar; Leena Kumari; Asit De; Tanmoy Bera
Journal:  Int J Nanomedicine       Date:  2017-07-07

3.  Manufacture and Physicochemical Properties of Chitosan Oligosaccharide/A2 β-Casein Nano-Delivery System Entrapped with Resveratrol.

Authors:  Mi Young Kim; Ho-Kyung Ha; Istifiani Lola Ayu; Kyoung-Sik Han; Won-Jae Lee; Mee-Ryung Lee
Journal:  Food Sci Anim Resour       Date:  2019-10-31

4.  Novel Strategy to Fabricate PLA/Au Nanocomposites as an Efficient Drug Carrier for Human Leukemia Cells in Vitro.

Authors:  Jingyuan Li; Chen Chen; Xuemei Wang; Zhongze Gu; Baoan Chen
Journal:  Nanoscale Res Lett       Date:  2010-09-14       Impact factor: 4.703

  4 in total

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