O'Brien C N, Guidry A J
Department of Animal Sciences, University of Maryland, College Park 20742, USA.
J Dairy Sci. 1996 Nov;79(11):1954-9. doi: 10.3168/jds.S0022-0302(96)76566-9.
This study determined optimal parameters for producing controlled-release microspheres and examined their suitability for vaccines via ingestion by bovine leukocytes. Microspheres elicit an immune response when ingested by antigen-presenting cells and provide sustained exposure of antigen to sensitized cells. Ingestion of microspheres is determined by their size (< 10 microns), and antigen release is governed by composition. Poly(DL-lactide-co-glycolide) microspheres were prepared using different polymer concentrations, stir rates, emulsifier concentrations, and emulsifier molecular masses. Microspheres that were < 10 microns were prepared using a 6% 50:50 lactide to glycolide polymer solution emulsified at 12,000 rpm in a low molecular mass, 5% polyvinyl alcohol solution. Microspheres that were > 20 microns were prepared using a 10% 85:15 lactide to glycolide polymer solution emulsified at 1200 rpm in a low molecular mass, 3% polyvinyl alcohol solution. Small microspheres released 90% of the antigen after 7 d, and large microspheres released only 24% of the antigen after 56 d. Both monocytes and neutrophils selectively ingested small microspheres that were opsonized with normal bovine serum (heated and unheated). Ingestion of microspheres that had been opsonized with fetal bovine serum (heated and unheated) was minimal. Lymphocytes did not ingest microspheres. Ingestion of small microspheres by bovine monocytes and sustained release of antigen by large microspheres suggested that microspheres have the ability to produce a sustained immune response with a single injection.
本研究确定了制备控释微球的最佳参数,并通过牛白细胞摄取来检验其对疫苗的适用性。微球被抗原呈递细胞摄取时会引发免疫反应,并使抗原持续暴露于致敏细胞。微球的摄取取决于其大小(<10微米),而抗原释放则由其组成决定。使用不同的聚合物浓度、搅拌速率、乳化剂浓度和乳化剂分子量制备了聚(DL-丙交酯-共-乙交酯)微球。使用6%的50:50丙交酯与乙交酯聚合物溶液,在低分子量的5%聚乙烯醇溶液中以12,000转/分钟的速度乳化,制备出了<10微米的微球。使用10%的85:15丙交酯与乙交酯聚合物溶液,在低分子量的3%聚乙烯醇溶液中以1200转/分钟的速度乳化,制备出了>20微米的微球。小微球在7天后释放了90%的抗原,而大微球在56天后仅释放了24%的抗原。单核细胞和中性粒细胞都选择性地摄取了用正常牛血清(加热和未加热)调理过的小微球。用胎牛血清(加热和未加热)调理过的微球摄取量极少。淋巴细胞不摄取微球。牛单核细胞对小微球的摄取以及大微球对抗原的持续释放表明,微球能够通过单次注射产生持续的免疫反应。