Techniques For The Preparation of Tissue Samples Containing Injectable Polymer Microcapsules

Author(s):  
G.E. Visscher ◽  
R. L. Robison ◽  
G. J. Argentieri

The use of various bioerodable polymers as drug delivery systems has gained considerable interest in recent years. Among some of the shapes used as delivery systems are films, rods and microcapsules. The work presented here will deal with the techniques we have utilized for the analysis of the tissue reaction to and actual biodegradation of injectable microcapsules. This work has utilized light microscopic (LM), transmission (TEM) and scanning (SEM) electron microscopic techniques. The design of our studies has utilized methodology that would; 1. best characterize the actual degradation process without artifacts introduced by fixation procedures and 2. allow for reproducible results.In our studies, the gastrocnemius muscle of the rat was chosen as the injection site. Prior to the injection of microcapsules the skin above the sites was shaved and tattooed for later recognition and recovery. 1.0 cc syringes were loaded with the desired quantity of microcapsules and the vehicle (0.5% hydroxypropylmethycellulose) drawn up. The syringes were agitated to suspend the microcapsules in the injection vehicle.

Author(s):  
G. E. Visscher ◽  
R. L. Robison ◽  
G. J. Argentieri

It was our goal to characterize the tissue response to and biodegradation of microcapsules of lypressin composed of two different polymers. Microcapsules of lypressin were made with the polymer 50:50 poly (DL-lactide-co-glycolide) DLPLGA and poly (D, L-lactide) DLPLA. The work which is presented here compares the in vivo characteristics of these microcapsules as drug delivery systems.For the study using DLPLGA, 14 groups of male rats were administered, as an intramuscular injection (gastrocnemius), microencapsulated lypressin (1%). Injections of microcapsules were examined through Day 63 of the experiment. In the second study using DLPLA, 27 male rats were injected with microcapsules of lypressin (0.4%) and examined at 30 day intervals through 420 days post injection. Light microscopy was used to characterize the tissue reaction to the injected microcapsules.


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