Lectin-conjugated PLGA nanoparticles loaded with thymopentin: Ex vivo bioadhesion and in vivo biodistribution

• Published in: Journal of controlled release 2007-10, Vol.123 (1), p.27-38
• Main Authors: Yin, YaShu, Chen, DaWei, Qiao, MingXi, Wei, XiuYan, Hu, HaiYang
• Format: Article
• Language: English
• Subjects: Animals; Bioadhesion; Biodistribution; Biological and medical sciences; General pharmacology; Intestinal Absorption - drug effects; Intestinal Absorption - physiology; Lactic Acid - chemistry; Lactic Acid - pharmacokinetics; Lectin; Medical sciences; Nanoparticles; Nanoparticles - chemistry; Oral uptake; Pharmaceutical technology. Pharmaceutical industry; Pharmacology. Drug treatments; Polyglycolic Acid - chemistry; Polyglycolic Acid - pharmacokinetics; Polymers - chemistry; Polymers - pharmacokinetics; Rats; Rats, Wistar; Thymopentin - chemistry; Thymopentin - pharmacokinetics; Tissue Distribution - drug effects; Tissue Distribution - physiology; Wheat germ agglutinin; Wheat Germ Agglutinins - chemistry; Wheat Germ Agglutinins - pharmacokinetics
• ISSN: 0168-3659; 1873-4995
• DOI: 10.1016/j.jconrel.2007.06.024

The conjugation of lectins onto PLGA nanoparticles has been demonstrated to effectively improve the intestinal absorption of thymopentin. In this study, thymopentin-loaded nanoparticles made from fluorescein isothiocyanate labeled PLGA were modified with wheat germ agglutinin (WGA). The specific bioadhesion of nanoparticles on rat intestinal mucosa was studied ex vivo. An important increase of interaction between WGA-conjugated nanoparticles and the intestinal segments was observed compared with that of the unconjugated one ( p < 0.05). Fluorescence photomicrographs confirmed the bioadhesion of WGA-conjugated nanoparticles on intestinal villous epithelium as well as Peyer's patches. Biodistribution of nanoparticles was evaluated using tissues obtained from rats, to which nanoparticles were orally administered. The highest amount of WGA-conjugated nanoparticles was detected in small intestine, suggesting an increase of intestinal bioadhesion and endocytosis. The systemic uptake was as high as 6.48–13.4% of dose at 1 day and 7.32–15.26% at 7 days, which representing an increase of almost 1.4–3.1 fold across the intestine compared to < 4.9% of the unconjugated one. The enhanced uptake was related to the increasing of WGA density on nanoparticles. These results further revealed the promising potential of lectin-conjugated nanoparticles on the improvement of intestinal bioadhesion and absorption for oral drug delivery.