Literature DB >> 34609731

Lipid-based emulsion drug delivery systems - a comprehensive review.

Mori Dhaval1, Poonam Vaghela2, Kajal Patel2, Keshvi Sojitra2, Mohini Patel2, Sushma Patel2, Kiran Dudhat3, Sunny Shah2, Ravi Manek2, Ramesh Parmar2.   

Abstract

Lipid-based emulsion system - a subcategory of emulsion technology, has emerged as an enticing option to improve the solubility of the steadily rising water-insoluble candidates. Along with enhancing solubility, additional advantages such as improvement in permeability, protection against pre-systemic metabolism, ease of manufacturing, and easy to scale-up have made lipid-based emulsion technology very popular among academicians and manufacturers. The present article provides a comprehensive review regarding various critical properties of lipid-based emulsion systems, such as microemulsion, nanoemulsion, SMEDDS (self microemulsifying drug delivery system), and SNEDDS (self nanoemulsifying drug delivery system). The present article also explains in detail the similarities and differences between them, the stabilization mechanism, methods of preparation, excipients used to prepare them, and evaluation techniques. Subtle differences between nearly related terminologies such as microemulsion and nanoemulsion, SMEDDS, and SNEDDS are also explained in detail to clarify the basic differences. The present article also gives in-depth information regarding the chemical structure of various lipidic excipients, various possible chemical modifications to modify their inherent properties, and their regulatory status for rational selection.
© 2021. Controlled Release Society.

Entities:  

Keywords:  Emulsification theory; Excipients; Method of manufacturing; Microemulsion; Nanoemulsion; SMEDDS; SNEDDS

Mesh:

Substances:

Year:  2021        PMID: 34609731     DOI: 10.1007/s13346-021-01071-9

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


  49 in total

Review 1.  Drug-like properties and the causes of poor solubility and poor permeability.

Authors:  C A Lipinski
Journal:  J Pharmacol Toxicol Methods       Date:  2000 Jul-Aug       Impact factor: 1.950

2.  Accuracy of calculated pH-dependent aqueous drug solubility.

Authors:  Christel A S Bergström; Kristina Luthman; Per Artursson
Journal:  Eur J Pharm Sci       Date:  2004-08       Impact factor: 4.384

Review 3.  Aqueous solubility of crystalline and amorphous drugs: Challenges in measurement.

Authors:  Sharad B Murdande; Michael J Pikal; Ravi M Shanker; Robin H Bogner
Journal:  Pharm Dev Technol       Date:  2010-04-30       Impact factor: 3.133

Review 4.  IV-IVC considerations in the development of immediate-release oral dosage form.

Authors:  Shoufeng Li; Handan He; Lakshman J Parthiban; Hequn Yin; Abu T M Serajuddin
Journal:  J Pharm Sci       Date:  2005-07       Impact factor: 3.534

Review 5.  Lipid-based systems as a promising approach for enhancing the bioavailability of poorly water-soluble drugs.

Authors:  Katja Cerpnjak; Alenka Zvonar; Mirjana Gašperlin; Franc Vrečer
Journal:  Acta Pharm       Date:  2013-12       Impact factor: 2.230

Review 6.  Improvement in aqueous solubility in small molecule drug discovery programs by disruption of molecular planarity and symmetry.

Authors:  Minoru Ishikawa; Yuichi Hashimoto
Journal:  J Med Chem       Date:  2011-02-23       Impact factor: 7.446

Review 7.  Oral lipid based drug delivery system (LBDDS): formulation, characterization and application: a review.

Authors:  Md Akhlaquer Rahman; Ranjit Harwansh; Mohd Aamir Mirza; Sarfaraj Hussain; Arshad Hussain
Journal:  Curr Drug Deliv       Date:  2011-07       Impact factor: 2.565

8.  Optimizing solubility: kinetic versus thermodynamic solubility temptations and risks.

Authors:  Christoph Saal; Anna Christine Petereit
Journal:  Eur J Pharm Sci       Date:  2012-08-03       Impact factor: 4.384

9.  Quantitative analysis of the effect of supersaturation on in vivo drug absorption.

Authors:  Ryusuke Takano; Noriyuki Takata; Ryoichi Saito; Kentaro Furumoto; Shoichi Higo; Yoshiki Hayashi; Minoru Machida; Yoshinori Aso; Shinji Yamashita
Journal:  Mol Pharm       Date:  2010-08-12       Impact factor: 4.939

10.  Effect of characteristics of compounds on maintenance of an amorphous state in solid dispersion with crospovidone.

Authors:  Yusuke Shibata; Makiko Fujii; Makiko Kokudai; Shinobu Noda; Hideko Okada; Masuo Kondoh; Yoshiteru Watanabe
Journal:  J Pharm Sci       Date:  2007-06       Impact factor: 3.534

View more
  3 in total

Review 1.  Recent Advance in Tumor Microenvironment-Based Stimuli-Responsive Nanoscale Drug Delivery and Imaging Platform.

Authors:  Fengzhi Cui; Jianhua Liu; Siwen Pang; Bo Li
Journal:  Front Pharmacol       Date:  2022-07-22       Impact factor: 5.988

2.  Enhanced oral absorption of insulin: hydrophobic ion pairing and a self-microemulsifying drug delivery system using a D-optimal mixture design.

Authors:  Yoon Tae Goo; Sangkil Lee; Ji Yeh Choi; Min Song Kim; Gi Hyeong Sin; Sun Ho Hong; Chang Hyun Kim; Seh Hyon Song; Young Wook Choi
Journal:  Drug Deliv       Date:  2022-12       Impact factor: 6.819

3.  Microemulsion Delivery System Improves Cellular Uptake of Genipin and Its Protective Effect against Aβ1-42-Induced PC12 Cell Cytotoxicity.

Authors:  Yujie Zheng; Guangzhi Xu; Qinxue Ni; Yan Wang; Qianxin Gao; Youzuo Zhang
Journal:  Pharmaceutics       Date:  2022-03-11       Impact factor: 6.321

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.