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Facile fabrication of diblock methoxy poly(ethylene glycol)-poly(tetramethylene carbonate) and its self-assembled micelles as drug carriers.
ACS Appl Mater Interfaces 2009; 1(12):2729-37AA

Abstract

AB type diblock methoxy poly(ethylene glycol)-b-poly(tetramethylene carbonate) (mPEG-PTeMC) copolymers were designed for the first time and used as carriers for the sustained release of the hydrophobic drug ibuprofen. In this paper, we developed a facile ring-opening polymerization (ROP) method to prepare mPEG-PTeMC copolymers under the catalysis of Novozym-435 lipase. Attractively, the polymerization has been successfully performed at 30 degrees C, close to room temperature. The data show that the copolymer compositions agree well with the feed ratio of TeMC to mPEG, indicating the controllable feature of the polymerization. The copolymer structures were characterized by (1)H NMR, IR, SEC, and DSC measurements. mPEG-PTeMC exhibits no apparent in vitro cytotoxicity toward human embryonic kidney transformed 293T cells. Those amphiphilic copolymers can readily self-assemble into nanosized micelles (about 150 nm) in aqueous solution. Their critical micelle concentrations are in the range of (1.6-9.3) x 10(-7) mol/L, determined by fluorescence spectroscopy. The micelles present high stability in PBS solution, with no obvious change in micelle diameters over 5 days. Ibuprofen can be loaded effectively in mPEG-PTeMC micelles, and its sustained release behavior is observed. Transmission electron microscopy shows that the well-dispersed spherical micelles are around 25 nm in diameter, while the diameter is 30 nm after loading ibuprofen. The release rate increases when the chain length of the PTeMC block decreases. These properties show that the micelles self-assembled from mPEG-PTeMC copolymers would have great potential as carriers for the effective encapsulation as well as sustained release of hydrophobic drugs.

Authors+Show Affiliations

Key Laboratory of Biomedical Polymers (The Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072, People's Republic of China. fengjun@whu.edu.cnNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

20356150

Citation

Feng, Jun, et al. "Facile Fabrication of Diblock Methoxy Poly(ethylene Glycol)-poly(tetramethylene Carbonate) and Its Self-assembled Micelles as Drug Carriers." ACS Applied Materials & Interfaces, vol. 1, no. 12, 2009, pp. 2729-37.
Feng J, Su W, Wang HF, et al. Facile fabrication of diblock methoxy poly(ethylene glycol)-poly(tetramethylene carbonate) and its self-assembled micelles as drug carriers. ACS Appl Mater Interfaces. 2009;1(12):2729-37.
Feng, J., Su, W., Wang, H. F., Huang, F. W., Zhang, X. Z., & Zhuo, R. X. (2009). Facile fabrication of diblock methoxy poly(ethylene glycol)-poly(tetramethylene carbonate) and its self-assembled micelles as drug carriers. ACS Applied Materials & Interfaces, 1(12), pp. 2729-37. doi:10.1021/am900452c.
Feng J, et al. Facile Fabrication of Diblock Methoxy Poly(ethylene Glycol)-poly(tetramethylene Carbonate) and Its Self-assembled Micelles as Drug Carriers. ACS Appl Mater Interfaces. 2009;1(12):2729-37. PubMed PMID: 20356150.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Facile fabrication of diblock methoxy poly(ethylene glycol)-poly(tetramethylene carbonate) and its self-assembled micelles as drug carriers. AU - Feng,Jun, AU - Su,Wei, AU - Wang,Hua-fen, AU - Huang,Fu-wei, AU - Zhang,Xian-zheng, AU - Zhuo,Ren-xi, PY - 2010/4/2/entrez PY - 2010/4/2/pubmed PY - 2010/4/23/medline SP - 2729 EP - 37 JF - ACS applied materials & interfaces JO - ACS Appl Mater Interfaces VL - 1 IS - 12 N2 - AB type diblock methoxy poly(ethylene glycol)-b-poly(tetramethylene carbonate) (mPEG-PTeMC) copolymers were designed for the first time and used as carriers for the sustained release of the hydrophobic drug ibuprofen. In this paper, we developed a facile ring-opening polymerization (ROP) method to prepare mPEG-PTeMC copolymers under the catalysis of Novozym-435 lipase. Attractively, the polymerization has been successfully performed at 30 degrees C, close to room temperature. The data show that the copolymer compositions agree well with the feed ratio of TeMC to mPEG, indicating the controllable feature of the polymerization. The copolymer structures were characterized by (1)H NMR, IR, SEC, and DSC measurements. mPEG-PTeMC exhibits no apparent in vitro cytotoxicity toward human embryonic kidney transformed 293T cells. Those amphiphilic copolymers can readily self-assemble into nanosized micelles (about 150 nm) in aqueous solution. Their critical micelle concentrations are in the range of (1.6-9.3) x 10(-7) mol/L, determined by fluorescence spectroscopy. The micelles present high stability in PBS solution, with no obvious change in micelle diameters over 5 days. Ibuprofen can be loaded effectively in mPEG-PTeMC micelles, and its sustained release behavior is observed. Transmission electron microscopy shows that the well-dispersed spherical micelles are around 25 nm in diameter, while the diameter is 30 nm after loading ibuprofen. The release rate increases when the chain length of the PTeMC block decreases. These properties show that the micelles self-assembled from mPEG-PTeMC copolymers would have great potential as carriers for the effective encapsulation as well as sustained release of hydrophobic drugs. SN - 1944-8244 UR - https://www.unboundmedicine.com/medline/citation/20356150/Facile_fabrication_of_diblock_methoxy_poly_ethylene_glycol__poly_tetramethylene_carbonate__and_its_self_assembled_micelles_as_drug_carriers_ L2 - https://dx.doi.org/10.1021/am900452c DB - PRIME DP - Unbound Medicine ER -