Selective cancer therapeutics最新文献

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Rapid remission of a large pleomorphic rhabdomyosarcoma with radiation and a novel schedule of simultaneous high-dose cisplatin. 大多形性横纹肌肉瘤的快速缓解与放疗和同时高剂量顺铂的新计划。
Selective cancer therapeutics Pub Date : 1989-01-01 DOI: 10.1089/sct.1989.5.205
W J Uphouse, Y T Lee, A P Ronquillo, K Fleet
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引用次数: 1
Effects of physiological oxygen environment on drug-induced cell lethality of multicellular tumor spheroids from human lung cancer. 生理氧环境对人肺癌多细胞肿瘤球体药物致死性的影响。
Selective cancer therapeutics Pub Date : 1989-01-01 DOI: 10.1089/sct.1989.5.13
S Inoue, T Ohnuma
{"title":"Effects of physiological oxygen environment on drug-induced cell lethality of multicellular tumor spheroids from human lung cancer.","authors":"S Inoue,&nbsp;T Ohnuma","doi":"10.1089/sct.1989.5.13","DOIUrl":"https://doi.org/10.1089/sct.1989.5.13","url":null,"abstract":"<p><p>Advanced malignant tumors of certain histological types contain a hypoxic and necrotic core. Multicellular tumor spheroids (MTS) have the characteristics of chronically hypoxic cells in the center. We studied the effects of physiological oxygen environment on MTS growth and the cell lethality produced by doxorubicin (DXR) and cisplatin (DDP). MTS were made from 2 human lung cancer cell lines; PC-6 small cell and PC-10 squamous cell carcinoma, and grown for 2, 3 or 4 weeks; either in 5% CO2/air or 5% 02/5% CO2/90% N2. They were exposed to graded concentrations of DXR for 1 hr and cell lethality was determined by clonogenic assay. In the physiological oxygen environment MTS growth was retarded for both cell lines. PC-6 MTS grown in physiological oxygen environment were more sensitive to DXR than those developed in air. The differential sensitivity was most pronounced with the 2 week old MTS and gradually narrowed with increasing MTS size. In contrast, PC-10 MTS developed in the physiological oxygen environment were more resistant to DXR than those in air; the differences were again most pronounced in 2 week old MTS. There were little differences in cell kill effects of DDP, irrespective of cells being in monolayer or in MTS and growing in air or in physiological oxygen environment. These observations are consistent with the interpretation that cells in PC-6 MTS are scarcely affected by the physiological oxygen environment but easily affected by DXR, whereas cells in PC-10 MTS responded vice versa.</p>","PeriodicalId":21792,"journal":{"name":"Selective cancer therapeutics","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1989-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/sct.1989.5.13","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13896300","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Biocompatibility of a biodegradable, controlled-release polymer in the rabbit brain. 一种可生物降解、控释聚合物在兔脑中的生物相容性。
Selective cancer therapeutics Pub Date : 1989-01-01 DOI: 10.1089/sct.1989.5.55
H Brem, A Kader, J I Epstein, R J Tamargo, A Domb, R Langer, K W Leong
{"title":"Biocompatibility of a biodegradable, controlled-release polymer in the rabbit brain.","authors":"H Brem,&nbsp;A Kader,&nbsp;J I Epstein,&nbsp;R J Tamargo,&nbsp;A Domb,&nbsp;R Langer,&nbsp;K W Leong","doi":"10.1089/sct.1989.5.55","DOIUrl":"https://doi.org/10.1089/sct.1989.5.55","url":null,"abstract":"<p><p>The biodegradable polyanhydrides are a new class of controlled release polymers developed for the interstitial delivery of drugs to their target site in the brain or other organs over periods ranging from days to years. These polymers can release molecules of any size in a predictable fashion. Their degradation products are non-cytotoxic and biocompatible. The biocompatibility of a biodegradable polyanhydride, the copolymer of poly[bis(p-carboxyphenoxy)propane] anhydride and sebacic acid (PCPP-SA) in a 50:50 formulation, was studied in the rabbit brain. Twenty adult New Zealand White male rabbits underwent implantation of PCPP-SA in a frontal lobe and absorbable gelatin sponge (Gelfoam) in the other frontal lobe. The animals were evaluated daily until the time of sacrifice. Groups of four animals were sacrificed sequentially on post-operative days 1, 3, 7, 21, and 60, and the brains processed for histological evaluation. None of the animals showed behavioral changes or neurological deficits suggestive of toxicity and all that received implants survived to their date of sacrifice. The histological examination showed no significant differences between the tissue reaction from PCPP-SA compared to Gelfoam. The polymers were also tested in the rabbit cornea bioassay and did not induce an inflammatory response. We conclude that PCPP-SA (50:50), a new biodegradable polymeric matrix that can be surgically implanted for the interstitial delivery of drugs in the brain, is biocompatible in the rabbit brain.</p>","PeriodicalId":21792,"journal":{"name":"Selective cancer therapeutics","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1989-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/sct.1989.5.55","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13911513","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 120
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