Chang T M
Artificial Cells and Organs Research Centre, Faculty of Medicine, McGill University, Montreal, Quebec, Canada.
Eur J Pharm Biopharm. 1998 Jan;45(1):3-8. doi: 10.1016/S0939-6411(97)00117-3.
Artificial cells for pharmaceutical and therapeutic applications started as microencapsulation on the micron scale. This has now expanded up to the higher range of macrocapsules and down to the nanometer range of nanocapsules and even to the macromolecular range of cross-linked hemoglobin as blood substitutes. This author first reported microencapsulation of biologically active material in 1957 (T.M.S. Chang, Hemoglobin corpuscles. Research Report for Honours Physiology, Medical Library, McGill University, 1957. (Also reprinted as part of 30th anniversary in Artificial Red Blood Cells Research, J. Biomater. Artif. Cells Artif. Organs 16 (1988) 1-9.) and 1964 (T.M.S. Chang, Semipermeable microcapsules, Science 146 (1964) 524-525). While pharmaceutical research has made use of these approaches for drug delivery, this author has been concentrating on the encapsulation of biotechnological products for therapeutic applications. Therefore, there was little interaction between the two approaches. In the last 10 years, pharmaceutical research, as in other areas of research, has become increasingly interested in biotechnology. Because of this interest, this article is a brief overview of developments of artificial cells for biotechnological products with emphasis on hemoglobin, enzymes, cells and genetically engineered microorganisms.
用于制药和治疗应用的人工细胞最初是微米级的微囊化技术。如今,这一技术已扩展到更大尺寸的大胶囊范围,也缩小到了纳米级的纳米胶囊范围,甚至延伸到了作为血液替代品的交联血红蛋白的大分子范围。本文作者于1957年首次报道了生物活性物质的微囊化(T.M.S. 张,血红蛋白微粒。麦吉尔大学医学图书馆荣誉生理学研究报告,1957年。(也作为《人工红细胞研究30周年》的一部分重印,《生物材料、人工细胞与人工器官》16 (1988) 1 - 9))以及1964年(T.M.S. 张,半透性微胶囊,《科学》146 (1964) 524 - 525)。虽然药物研究已将这些方法用于药物递送,但本文作者一直专注于生物技术产品的微囊化用于治疗应用。因此,这两种方法之间几乎没有相互作用。在过去十年中,与其他研究领域一样,药物研究对生物技术越来越感兴趣。基于这种兴趣,本文简要概述了用于生物技术产品的人工细胞的发展,重点是血红蛋白、酶、细胞和基因工程微生物。