{"title":"Use of perfluorochemical emulsions in cancer therapy.","authors":"B A Teicher","doi":"10.3109/10731199209119734","DOIUrl":null,"url":null,"abstract":"<p><p>Over the past 10 years, the use of perfluorochemical emulsions (PFCE) and carbogen or oxygen breathing has been explored as an adjuvant to radiation therapy and/or chemotherapy in the treatment of solid tumors. The rationale for the use of PFCE and oxygen breathing in this therapeutic setting is that solid tumor masses contain areas of hypoxia which are therapeutically resistant. Since x-rays and many chemotherapeutic agents require oxygen to be maximally cytotoxic and most normal tissues are well-oxygenated, the additional oxygen put in circulation by the PFCE should not increase the normal tissue toxicities produced by the various therapies. The largest body of preclinical work and all of the clinical studies in cancer conducted with PFCE, thus far, have been done with Fluosol-DA, 20%. Oxygen microelectrode studies have confirmed increased oxygenation in previously hypoxic tumor regions after the administration of Fluosol-DA and carbogen breathing. The preclinical studies have shown very positive effects with single dose and fractionated radiation in several rodent solid tumor models. Many widely used anticancer drugs including antitumor alkylating agents and adriamycin are enhanced by PFCE and carbogen breathing for longer time periods (6 h). More recently, several experimental concentrated PFCE preparations have become available and work with these is actively under way in several laboratories. Clinical studies with radiation and four or five chemotherapeutic drugs as single agents have indicated that Fluosol-DA followed by oxygen breathing can be administered safely in a variety of cancer therapeutic settings. Further clinical studies with Fluosol-DA are planned.</p>","PeriodicalId":77039,"journal":{"name":"Biomaterials, artificial cells, and immobilization biotechnology : official journal of the International Society for Artificial Cells and Immobilization Biotechnology","volume":"20 2-4","pages":"875-82"},"PeriodicalIF":0.0000,"publicationDate":"1992-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/10731199209119734","citationCount":"19","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomaterials, artificial cells, and immobilization biotechnology : official journal of the International Society for Artificial Cells and Immobilization Biotechnology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3109/10731199209119734","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 19

Abstract

Over the past 10 years, the use of perfluorochemical emulsions (PFCE) and carbogen or oxygen breathing has been explored as an adjuvant to radiation therapy and/or chemotherapy in the treatment of solid tumors. The rationale for the use of PFCE and oxygen breathing in this therapeutic setting is that solid tumor masses contain areas of hypoxia which are therapeutically resistant. Since x-rays and many chemotherapeutic agents require oxygen to be maximally cytotoxic and most normal tissues are well-oxygenated, the additional oxygen put in circulation by the PFCE should not increase the normal tissue toxicities produced by the various therapies. The largest body of preclinical work and all of the clinical studies in cancer conducted with PFCE, thus far, have been done with Fluosol-DA, 20%. Oxygen microelectrode studies have confirmed increased oxygenation in previously hypoxic tumor regions after the administration of Fluosol-DA and carbogen breathing. The preclinical studies have shown very positive effects with single dose and fractionated radiation in several rodent solid tumor models. Many widely used anticancer drugs including antitumor alkylating agents and adriamycin are enhanced by PFCE and carbogen breathing for longer time periods (6 h). More recently, several experimental concentrated PFCE preparations have become available and work with these is actively under way in several laboratories. Clinical studies with radiation and four or five chemotherapeutic drugs as single agents have indicated that Fluosol-DA followed by oxygen breathing can be administered safely in a variety of cancer therapeutic settings. Further clinical studies with Fluosol-DA are planned.

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全氟化学乳剂在癌症治疗中的应用。
在过去的10年里,人们探索了使用全氟化学乳剂(PFCE)和碳或氧呼吸作为辅助放射治疗和/或化疗治疗实体瘤的方法。在这种治疗环境中使用PFCE和氧气呼吸的基本原理是,实体肿瘤肿块包含缺氧区域,对治疗有抵抗性。由于x射线和许多化疗药物需要氧气来最大限度地发挥细胞毒性,而大多数正常组织都是充氧良好的,因此PFCE进入循环的额外氧气不应该增加各种疗法产生的正常组织毒性。迄今为止,使用PFCE进行的最大的临床前工作和所有癌症临床研究都是使用氟索洛- da进行的,占20%。氧微电极研究证实,在给予氟索- da和碳呼吸后,先前缺氧的肿瘤区域的氧合增加。临床前研究表明,单剂量和分次辐射对几种啮齿动物实体瘤模型有很好的效果。许多广泛使用的抗癌药物,包括抗肿瘤烷化剂和阿霉素,都可以通过PFCE和更长时间(6小时)的碳呼吸来增强。最近,几种实验性的浓缩PFCE制剂已经可用,并且在几个实验室中正在积极地进行研究。以放射和四到五种化疗药物作为单一药物的临床研究表明,在各种癌症治疗环境中,氟索- da加氧呼吸可以安全使用。Fluosol-DA的进一步临床研究正在计划中。
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Polysaccharide microcapsules and macroporous beads for enhanced chromatographic separation. Polydisperse dextran as a diffusing test solute to study the membrane permeability of alginate polylysine microcapsules. Inhibition of endotoxin-mediated activation of endothelial cells by a perfluorocarbon emulsion. Proceedings of the 2nd Bioencapsulation Research Group Workshop. Cachan, France, April 6-8, 1992. The use of semifluorinated alkanes in blood-substitutes.
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