A resorbable polymeric microreservoir device for controlled release drug delivery

The method by which a drug is delivered can have a significant effect on the drug's therapeutic efficacy. Pulsatile delivery of certain drugs and molecules (such as hormones) has been shown to more efficacious than continuous delivery, as the fluctuation in concentration levels in vivo more closely mimics the natural physiological processes of the human body. However, there is a shortage of systems that are capable of delivering drugs in this manner, particularly if it is desired to have a self-contained system that does not require external stimulation to trigger device function. The objectives of this thesis were to design, fabricate, test, and characterize a biodegradable polymeric microreservoir device that is capable of delivering multiple pulses of drugs in a reproducible manner. This polymeric microreservoir device contains an array of reservoirs that are each covered by a thin membrane of a degradable polymer. Control over the release of drugs from the device was achieved by changing the molecular weight of the reservoir membranes. The current prototypes have 36 reservoirs, but the size and geometry of the polymeric chip could be designed to optimize device performance depending on the application for which it will be used. Changing the membrane materials or thicknesses could change the time at which the chemicals are released from the reservoirs. Each reservoir on the device could potentially have a different set of membrane characteristics, enabling release of the contents of each reservoir at a different time. A fabrication process for these devices was developed, that consists of two compression-molding steps, followed by microinjection of the reservoir membranes from solution and subsequent drying of the membranes under vacuum and elevated temperature. The devices are then loaded with the drugs to be released and sealed at room temperature. This fabrication process avoids exposure of the drugs to solvents and high temperatures that may adversely affect their stability. Further, the compression-molding process used to fabricate the main body of the device, as well as minimal solvent used in the fabrication of the reservoir membranes, were designed to minimize adverse effects upon in vivo implantation due to residual solvent. Poly(L-lactic acid) was selected as the component material for the device substrate, while

Department dc:contributor.department

Massachusetts Institute of Technology. Dept. of Materials Science and Engineering.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2003

Author dc:creator

• Grayson, Amy Catherine Richards, 1975-

Advisor dc:contributor.advisor

• Robert S. Langer and Michael J. Cima.

• Materials Science and Engineering.

Statement dc:rights

• M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/17036

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/17036