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Lactic/glycolic acid polymers as narcotic antagonist delivery systems.

作者信息

Schwope A D, Wise D L, Howes J F

出版信息

Life Sci. 1975 Dec 15;17(12):1877-85. doi: 10.1016/0024-3205(75)90473-7.

DOI:10.1016/0024-3205(75)90473-7
PMID:1241097
Abstract
摘要

相似文献

1
Lactic/glycolic acid polymers as narcotic antagonist delivery systems.
Life Sci. 1975 Dec 15;17(12):1877-85. doi: 10.1016/0024-3205(75)90473-7.
2
Development of polylactic/glycolic acid delivery systems for use in treatment of narcotic addiction.
Natl Inst Drug Abuse Res Monogr Ser. 1975(4):13-8.
3
Development of polylactic/glycolic acid delivery systems for use in treatment of narcotic addiction.
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Development of injectable microcapsules for use in the treatment of narcotic addiction.
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5
Long acting delivery systems for narcotic antagonists II: release rates of naltrexone from poly(lactic acid) composites.麻醉拮抗剂长效给药系统II：纳曲酮从聚乳酸复合材料中的释放速率
J Pharm Sci. 1975 Feb;64(2):348-9. doi: 10.1002/jps.2600640239.
6
Development of Chronomers for narcotic antagonists.
Natl Inst Drug Abuse Res Monogr Ser. 1975(4):39-42.
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Testing of drug delivery systems for use in the treatment of narcotic addiction.用于治疗麻醉品成瘾的药物递送系统的测试。
Natl Inst Drug Abuse Res Monogr Ser. 1975(4):43-5.
8
The effects of naltrexone on the development of physical dependence on morphine.
Eur J Pharmacol. 1978 Aug 1;50(3):193-202. doi: 10.1016/0014-2999(78)90351-5.
9
Use of synthetic polypeptides in the preparation of biodegradable delivery vehicles for narcotic antagonists.
Natl Inst Drug Abuse Res Monogr Ser. 1975(4):33-8.
10
Effects of ICI204,448, naloxone methiodide and levocetirizine on the scratching behavior induced by a κ-opioid antagonist, nor-BNI, in ICR mice.ICI204,448、甲硫碘化纳洛酮和左西替利嗪对ICR小鼠中由κ-阿片受体拮抗剂nor-BNI诱导的抓挠行为的影响。
Immunopharmacol Immunotoxicol. 2017 Oct;39(5):292-295. doi: 10.1080/08923973.2017.1354879. Epub 2017 Jul 26.

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Shape dependent cytotoxicity of PLGA-PEG nanoparticles on human cells.PLGA-PEG 纳米粒的形貌依赖性人细胞毒性。
Sci Rep. 2017 Aug 4;7(1):7315. doi: 10.1038/s41598-017-07588-9.
2
Studies on in vitro availability, degradation, and thermal properties of naltrexone-loaded biodegradable microspheres.载纳曲酮可生物降解微球的体外释放度、降解和热性能研究。
Drug Dev Ind Pharm. 2011 Jun;37(6):673-84. doi: 10.3109/03639045.2010.535540. Epub 2011 Mar 30.
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Sustained-release naltrexone for opioid dependence.用于阿片类药物依赖的缓释纳曲酮
Cochrane Database Syst Rev. 2008 Apr 16(2):CD006140. doi: 10.1002/14651858.CD006140.pub2.
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Development and characterization of microencapsulated microspheres.
Pharm Res. 1994 Nov;11(11):1568-74. doi: 10.1023/a:1018901619230.
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[Release delay of various antibiotics from resorbable tricalcium phosphate ceramic granules with soluble coating for local treatment of osteomyelitis. An animal experiment study].[用于骨髓炎局部治疗的具有可溶涂层的可吸收磷酸三钙陶瓷颗粒对多种抗生素的释放延迟。一项动物实验研究]
Langenbecks Arch Chir. 1983;360(3):193-206. doi: 10.1007/BF01259235.
6
Pharmacokinetic quantitation of naltrexone controlled release from a copolymer delivery system.从共聚物给药系统中释放的纳曲酮控释的药代动力学定量分析。
J Pharmacokinet Biopharm. 1983 Aug;11(4):369-87. doi: 10.1007/BF01058956.
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The preparation and evaluation of drug-containing poly(dl-lactide) microspheres formed by the solvent evaporation method.通过溶剂蒸发法制备含药聚（dl-丙交酯）微球及其评价
Pharm Res. 1987 Dec;4(6):465-71. doi: 10.1023/a:1016419303727.