Enhancement by perflusion emulsion (Oxygent) and carbogen breathing of the tumor growth delay of the FSaIIC fibrosarcoma after treatment with antitumor alkylating agents.

S A Holden, B A Teicher, C Ha, G Ara, T S Herman
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引用次数: 11

Abstract

Many anticancer drugs require oxygen to be cytotoxic, or are selectively cytotoxic toward cells under oxygenated conditions. The effects of the dilute perfluorochemical emulsion Fluosol-DA with a wide variety of chemotherapeutic agents have been explored; however, it has not been possible to determine the optimal level of circulating perfluorochemical emulsion with anticancer drugs because the volume of Fluosol that may be administered in limited. Using a concentrated 90% Perflubron emulsion, Oxygent, a wide range of perfluorochemical emulsion doses have been examined in combination with melphalan, cyclophosphamide and BCNU in a murine solid tumor model. When Oxygent was administered by injection i.v. just prior to the injection of melphalan (10 mg/kg), the greatest tumor growth delays were obtained with Oxygent levels between 4 and 12 g PFC/kg. With each of these drugs the greatest tumor growth delays were obtained when the drug was prepared in the emulsion and the combination injected i.v. In each case, each dose of drug was followed by 6 h. of breathing carbogen.

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抗肿瘤烷化剂治疗FSaIIC纤维肉瘤后,灌注乳剂(氧)和碳呼吸对肿瘤生长延迟的增强作用。
许多抗癌药物需要氧气才能产生细胞毒性,或者在氧化条件下对细胞有选择性的细胞毒性。探讨了稀释的全氟化学乳剂氟索- da与多种化疗药物的作用;然而,由于可施用的氟醇量有限,因此不可能确定含有抗癌药物的全氟化学乳剂的最佳循环剂量。使用浓缩的90%全氟化学乳剂,氧合剂,在小鼠实体瘤模型中研究了与美法兰、环磷酰胺和BCNU联合使用的大范围全氟化学乳剂剂量。在注射美法兰(10mg /kg)之前静脉注射Oxygent,当氧含量在4 - 12g PFC/kg之间时,肿瘤生长延迟最大。每一种药物在乳剂中制备并联合静脉注射时,肿瘤生长延迟最大。在每种情况下,每剂量药物后都有6小时的呼吸碳。
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