Tri-component copolymer rods as an implantable reservoir drug delivery system for constant and controllable drug release rate
Copolymers of (D,L-lactide-random-ε-caprolactone)-block-poly(ethylene glycol)-block-(D,L-lactide-random-ε-caprolactone) (PLECs) were synthesized with varied D,L-lactide (LA) content and different molecular weights (20 and 50 kDa). Polymer ratios, particularly the content of LA, had significant effect on the release of trypan blue. A lower trypan blue release rate was observed from monolithic rods composed of PLECs with higher CL/LA ratio. High LA content in polymer rod led to increase of the hydrophilicity of the polymer rod and the decrease of CL content resulted in the increase of the hydrophilicity of PLECs and hydrolysis rate. Spin-coating technique was employed to coat PCL-b-PEG-b-PCL membrane on PLEC rod with controlled thickness. Results showed that membrane encased rods can produce different release pattern including delayed release, zero-ordered release and burst release depending on the types of inner rod and membrane. Results for this study indicated that PLEC rods could provide the zero-order release profile of highly water-soluble molecules. Moreover, the longer lag phase was observed at higher thickness. These results suggest that these polymer rods were potential drug delivery systems that can provide controlled drug release profiles.
KeywordsDrug delivery systems Polymer rods Biodegradable polymers Controllable drug release rate Reservoir drug delivery system
This work was supported by Thailand Research Fund (TRF) and Commission of Higher Education (CHE) for Norased Nasongkla. Financial support for Tararat Chanlen from the Center of Excellence for Innovation in Chemistry (PERCH-CIC), Office of the Higher Education Commission, Ministry of Education is gratefully acknowledged. We are thankful to Pat Akarajirathun for technical help.
- 1.Gliadel wafers for treatment of brain tumors (1998) Med Lett Drugs Ther 40(1035):92Google Scholar
- 8.Baker RW (1987) In: Controlled release of biologically active agents. Wiley, New YorkGoogle Scholar
- 18.Dash S, Murthy PN, Nath L, Chowdhury P (2010) Kinetic modeling on drug release from controlled drug delivery systems. Acta Poloniae Pharm—Drug Res 67(3):217–223Google Scholar