Improving anti-tumor activity with polymeric micelles entrapping paclitaxel in pulmonary carcinoma
- Authors
- Gong, C., Xie, Y., Wu, Q., Wang, Y., Deng, S., Xiong, D., Liu, L., Xiang, M., Qian, Z., and Wei, Y.
- ID
- ZDB-PUB-120823-2
- Date
- 2012
- Source
- Nanoscale 4(19): 6004-6017 (Journal)
- Registered Authors
- Keywords
- none
- MeSH Terms
-
- Animals
- Antineoplastic Agents, Phytogenic/administration & dosage*
- Antineoplastic Agents, Phytogenic/pharmacokinetics
- Antineoplastic Agents, Phytogenic/toxicity
- Carcinoma/drug therapy*
- Cell Line, Tumor
- Cell Survival/drug effects
- Disease Models, Animal
- Drug Carriers/chemistry*
- Fluorescein-5-isothiocyanate/chemistry
- Injections, Intravenous
- Injections, Subcutaneous
- Lung Neoplasms/drug therapy*
- Mice
- Mice, Inbred C57BL
- Micelles*
- Paclitaxel/administration & dosage*
- Paclitaxel/pharmacokinetics
- Paclitaxel/toxicity
- Polyesters/chemistry*
- Polyethylene Glycols/chemistry*
- Tissue Distribution
- Zebrafish
- PubMed
- 22910790 Full text @ Nanoscale
Nanoscale polymeric micelles have promising applications as drug delivery systems (DDS). In this work, to improve the anti-tumor activity and eliminate toxicity of the commercial formulation (cremophor EL and ethanol) of paclitaxel (PTX), we developed biodegradable poly(ethylene glycol)-poly(μ-caprolactone) (MPEG-PCL) micelles entrapping PTX by a simple one-step solid dispersion method, which is without any surfactants or additives and is easy to scale up. In addition, the PTX micelles could be lyophilized into powder without any adjuvant and the re-dissolved PTX micelles are stable and homogeneous. The prepared PTX micelles have a mean particle size of 38.06 ± 2.30 nm, a polydispersity index of 0.168 ± 0.014, a drug loading of 14.89 ± 0.06% and an encapsulation efficiency of 99.25 ± 0.38%. A molecular modeling study implied that PTX interacted with PCL as a core, which was embraced by PEG as a shell. The encapsulation of PTX in polymeric micelles enhanced its cytotoxicity by increasing the uptake by LL/2 cells. A sustained in vitro release behavior and slow extravasation behavior from blood vessels in a transgenic zebrafish model were observed in the PTX micelles. Furthermore, compared with Taxol®, the PTX micelles were more effective in suppressing tumor growth in the subcutaneous LL/2 tumor model. The PTX micelles also inhibited metastases in the pulmonary metastatic LL/2 tumor model and prolonged survival in both mouse models. Pharmacokinetic and tissue distribution studies showed that after PTX was encapsulated in polymeric micelles, the biodistribution pattern of PTX was altered and the PTX concentration in tumors was increased compared with Taxol® after intravenous injection. In conclusion, we have developed a polymeric micelles entrapping PTX that enhanced cytotoxicity in vitro and improved anti-tumor activity in vivo with low systemic toxicity on pulmonary carcinoma. The biodegradable MPEG-PCL micelles entrapping PTX may have promising applications in pulmonary carcinoma therapy.