Literature DB >> 26891912

Improved delivery of poorly soluble compounds using nanoparticle technology: a review.

Sandeep Kalepu1, Vijaykumar Nekkanti2.   

Abstract

Although a large number of new drug molecules with varied therapeutic potentials have been discovered in the recent decade, yet most of them are still in developmental process. This can be attributed to the limited aqueous solubility which governs the bioavailability of such drug molecules. Hence, there is a requisite for a technology-based product (formulation) in order to overcome such issues without compromising on the therapeutic response. The purpose of this review is to provide an insight to the formulation of drug nanoparticles for enhancing solubility and dissolution velocity with concomitant enhancement in bioavailability. In the recent decade, nanonization has evolved from a concept to reality owing to its versatile applications, especially in the development of drugs having poor solubility. In this review, a relatively simple and scalable approach for the manufacture of drug nanoparticles and latest characterization techniques utilized to evaluate the drug nanoparticles are discussed. The drug nanoparticulate approach described herein provides a general applicability of the platform technology in designing a formulation for drugs associated with poor aqueous solubility.

Keywords:  Dissolution rate; Drug nanoparticles; Homogenization; Particle size; Solid intermediate

Mesh:

Year:  2016        PMID: 26891912     DOI: 10.1007/s13346-016-0283-1

Source DB:  PubMed          Journal:  Drug Deliv Transl Res        ISSN: 2190-393X            Impact factor:   4.617


  29 in total

1.  Lab-scale production unit design for nanosuspensions of sparingly soluble cytotoxic drugs.

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Journal:  AAPS PharmSci       Date:  1999

4.  Comparative in vitro evaluation of several colloidal systems, nanoparticles, nanocapsules, and nanoemulsions, as ocular drug carriers.

Authors:  P Calvo; J L Vila-Jato; M J Alonso
Journal:  J Pharm Sci       Date:  1996-05       Impact factor: 3.534

Review 5.  Drug nanocrystals of poorly soluble drugs produced by high pressure homogenisation.

Authors:  Cornelia M Keck; Rainer H Müller
Journal:  Eur J Pharm Biopharm       Date:  2005-08-29       Impact factor: 5.571

6.  Liposome formulation of poorly water soluble drugs: optimisation of drug loading and ESEM analysis of stability.

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Journal:  Int J Pharm       Date:  2004-11-05       Impact factor: 5.875

7.  Using USP I and USP IV for discriminating dissolution rates of nano- and microparticle-loaded pharmaceutical strip-films.

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Journal:  AAPS PharmSciTech       Date:  2012-10-23       Impact factor: 3.246

8.  Novel, dynamic on-line analytical separation system for dissolution of drugs from poly(lactic acid) nanoparticles.

Authors:  Anne Helle; Samuli Hirsjärvi; Leena Peltonen; Jouni Hirvonen; Susanne K Wiedmer; Tuulia Hyötyläinen
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9.  Contribution of lymphatically transported testosterone undecanoate to the systemic exposure of testosterone after oral administration of two andriol formulations in conscious lymph duct-cannulated dogs.

Authors:  David M Shackleford; W A Faassen; Natalie Houwing; Holger Lass; Glenn A Edwards; Christopher J H Porter; William N Charman
Journal:  J Pharmacol Exp Ther       Date:  2003-06-13       Impact factor: 4.030

Review 10.  Nanocrystal technology, drug delivery and clinical applications.

Authors:  Jens-Uwe A H Junghanns; Rainer H Müller
Journal:  Int J Nanomedicine       Date:  2008
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  10 in total

Review 1.  Long acting systemic HIV pre-exposure prophylaxis: an examination of the field.

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Journal:  Drug Deliv Transl Res       Date:  2017-12       Impact factor: 4.617

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Authors:  Betty Annie Samuel; Bassim I Mohammed; Anil K Philip
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5.  Amino functionalized chiral mesoporous silica nanoparticles for improved loading and release of poorly water-soluble drug.

Authors:  Xin Wang; Chang Li; Na Fan; Jing Li; Haotian Zhang; Lei Shang; Zhonggui He; Jin Sun
Journal:  Asian J Pharm Sci       Date:  2018-07-01       Impact factor: 6.598

6.  Integration of phospholipid-drug complex into self-nanoemulsifying drug delivery system to facilitate oral delivery of paclitaxel.

Authors:  Dawei Ding; Bingjun Sun; Weiping Cui; Qin Chen; Xuanbo Zhang; Haotian Zhang; Zhonggui He; Jin Sun; Cong Luo
Journal:  Asian J Pharm Sci       Date:  2018-11-20       Impact factor: 6.598

Review 7.  Amino Acids as the Potential Co-Former for Co-Crystal Development: A Review.

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Journal:  Molecules       Date:  2021-05-28       Impact factor: 4.411

Review 8.  Pharmaceutical Dispersion Techniques for Dissolution and Bioavailability Enhancement of Poorly Water-Soluble Drugs.

Authors:  Xingwang Zhang; Huijie Xing; Yue Zhao; Zhiguo Ma
Journal:  Pharmaceutics       Date:  2018-06-23       Impact factor: 6.321

9.  Application of Box-Behnken Design to Investigate the Effect of Process Parameters on the Microparticle Production of Ethenzamide through the Rapid Expansion of the Supercritical Solutions Process.

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Journal:  Pharmaceutics       Date:  2020-01-03       Impact factor: 6.321

10.  Hydrophilic and Functionalized Nanographene Oxide Incorporated Faster Dissolving Megestrol Acetate.

Authors:  Mohammad Saiful Islam; Faradae Renner; Kimberly Foster; Martin S Oderinde; Kevin Stefanski; Somenath Mitra
Journal:  Molecules       Date:  2021-03-31       Impact factor: 4.411

  10 in total

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