Hadlock Tessa A, Sheahan Timothy, Cheney Mack L, Vacanti Joseph P, Sundback Cathryn A
Division of Facial Plastic and Reconstructive Surgery, Department of Otolaryngology/Head and Neck Surgery, Massachusetts Eye and Ear Infirmary, Boston, MA 02114, USA.
J Reconstr Microsurg. 2003 Apr;19(3):179-84; discussion 185-6. doi: 10.1055/s-2003-39831.
Efficient and sustained delivery of neurotrophic factors to the regenerating nerve in biologically active form presents a challenge. Protein delivery in biodegradable microsphere vehicles has been difficult, based on destabilization and breakdown during both the loading and release phases. This study examines the extravasation and stability of Nerve Growth Factor (NGF) in polylactic-co-glycolic acid (PLGA) microspheres, via both ELISA and PC-12 bioassays. PLGA microspheres co-loaded with bovine serum albumin (BSA) and NGF were prepared by a water-in-oil-in-water (W/O/W) technique, using chloroform for the organic phase and 1 percent polyvinyl alcohol (PVA) for the emulsion step. Aliquots of lyophilized microspheres were incubated in double distilled water (dd H2O) at 37 degrees C, and the supernatants assayed over time for NGF activity. ELISA was utilized for quantitative determination of NGF concentration, and a PC-12 cell neurite outgrowth assay assessed biologic activity. Both ELISA and PC-12 assays demonstrated the extravasation of NGF from microspheres. Over time, the predicted concentration of NGF via the two assays differed, suggesting possible preservation of recognizable epitopes for ELISA, but loss of biologic activity. NGF can be stored and released from microspheres. Extravasation studies should include biologically relevant assays for activity.
以生物活性形式将神经营养因子高效且持续地递送至再生神经是一项挑战。基于在装载和释放阶段的不稳定和分解,在可生物降解微球载体中进行蛋白质递送一直很困难。本研究通过酶联免疫吸附测定(ELISA)和PC-12生物测定法,研究了神经生长因子(NGF)在聚乳酸-乙醇酸共聚物(PLGA)微球中的渗出和稳定性。采用水包油包水(W/O/W)技术,以氯仿为有机相,1%聚乙烯醇(PVA)为乳化步骤,制备了同时负载牛血清白蛋白(BSA)和NGF的PLGA微球。将冻干微球的等分试样在37℃的双蒸水(dd H2O)中孵育,并随时间对上清液进行NGF活性测定。ELISA用于定量测定NGF浓度,PC-12细胞神经突生长测定评估生物活性。ELISA和PC-12测定均证明了NGF从微球中的渗出。随着时间的推移,通过这两种测定法预测的NGF浓度有所不同,这表明ELISA可能保留了可识别的表位,但生物活性丧失。NGF可以从微球中储存和释放。渗出研究应包括生物活性相关测定。