Long-circulating and target-specific distributions of cyanine 5.5-labeled hyaluronic acid nanoparticles in mouse organs during 28 days after a single administration
10.14405/kjvr.2018.58.4.183
- Author:
Tae Sik YUN
1
;
Chunmei LIN
;
Jung Min YON
;
Seul Gi PARK
;
Lee Wha GWON
;
Jong Geol LEE
;
In Jeoung BAEK
;
Sang Seop NAHM
;
Beom Jun LEE
;
Young Won YUN
;
Sang Yoon NAM
Author Information
1. College of Veterinary Medicine and Veterinary Medical Center, Chungbuk National University, Cheongju 28644, Korea. synam@cbu.ac.kr
- Publication Type:Original Article
- Keywords:
drug delivery systems;
hyaluronic acid;
nanoparticles;
tissue distribution;
toxicokinetics
- MeSH:
Animals;
Drug Delivery Systems;
Fluorescence;
Hyaluronic Acid;
Kidney;
Liver;
Lung;
Lymph Nodes;
Mice;
Nanoparticles;
Pharmacokinetics;
Spleen;
Sublingual Gland;
Testis;
Tissue Distribution;
Toxicokinetics
- From:Korean Journal of Veterinary Research
2018;58(4):183-192
- CountryRepublic of Korea
- Language:English
-
Abstract:
Although hyaluronic acid (HA) has been developed as a nanoparticle (NP; 320–400 nm) for a drug delivery system, the tissue targeting efficacy and the pharmacokinetics of HA-NPs are not yet fully understood. After a dose of 5 mg/kg of cyanine 5.5-labeled HA-NPs or HA-polymers was intravenously administrated into mice, the fluorescence was measured from 0.5 h to 28 days. The HA-NPs fluorescence was generally stronger than that of HA-polymers, which was maintained at a high level over 7 days in vivo, after which it gradually decreased. Upon ex vivo imaging, liver, spleen, kidney, lung, testis and sublingual gland fluorescences were much higher than that of other organs. The fluorescence of HA-NPs in the liver, spleen and kidney was highest at 30 min, where it was generally maintained until 4 h, while it drastically decreased at 1 day. However, the fluorescence in the liver and spleen increased sharply at 7 days relative to 3 days, then decreased drastically at 14 days. Conversely, the fluorescence of HA-polymers in the lymph node was higher than that of HA-NPs. The results presented herein may have important clinical implications regarding the safety of as self-assembled HA-NPs, which can be widely used in biomedical applications.
