Major difference in particle size, minor difference in release profile: a case study of solid lipid nanoparticles. (26th November 2021)

• Record Type: Journal Article
• Authors: Huang, Zhengwei; Wu, Linjing; Wang, Wenhao; Wang, Wenhua; Fu, Fangqin; Zhang, Xuejuan; Huang, Ying; Pan, Xin; Wu, Chuanbin
• Is Part Of: Pharmaceutical development and technology. Volume 26:Number 10(2021)
• Page Start: 1110
• Page End: 1119
• Publication Date: 2021-11-26
• Subjects: Particle size -- release profile -- solid lipid nanoparticle -- budesonide -- aggregation caused quenching; Drug delivery systems -- Periodicals; Pharmaceutical technology -- Periodicals; Drugs -- Administration -- Research -- Periodicals; Drug Delivery Systems -- Periodicals; Pharmaceutical Preparations -- Periodicals; Technology, Pharmaceutical -- Periodicals; 615
• DOI: 10.1080/10837450.2021.1998114
• Languages: English
• ISSNs: 1083-7450

Abstract

Abstract: Solid lipid nanoparticles (SLN) have been widely used in a variety of drug delivery routes, which have the outstanding advantage of controlled drug release. The release of SLN is dominated by many factors, among which the particle size of SLN is a critical one. The aim of this project was to explore the relationship between drug release profile and particle size of SLN. SLN were synthesized via the hot high-pressure homogenization (HPH) method, budesonide (BUD) was used as the model drug, and BUD-SLN1–BUD-SLN4 with increasing particle size was obtained, i.e. 120, 240, 360, and 480 nm. The prepared SLN has good encapsulation efficiency, drug loading capacity, and stability. In vitro release behavior studies showed that the cumulative release of BUD-SLN in Tris-Maleate (Tris-M) media was negligible, while that in Tris-M plus pancreatin media or Tris-M-ethanol media obeyed Ritger-Peppas model or first-order kinetic model, respectively. Noticeably, the release behavior of SLN was to some extent related to the average particle size of SLN, but the correlation was insignificant when the intersection degree of particle size distribution was great. This study provides a new idea for the understanding of in vitro release of SLN and has a certain referencing value for the research and development of novel nanomedicines.