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Formulation design and development of parenteral suspensions.

作者信息

Akers M J, Fites A L, Robison R L

出版信息

J Parenter Sci Technol. 1987 May-Jun;41(3):88-96.

PMID:3612415
Abstract
摘要

相似文献

1
Formulation design and development of parenteral suspensions.注射用混悬剂的处方设计与研发
J Parenter Sci Technol. 1987 May-Jun;41(3):88-96.
2
[Standard prescriptions for the formulation of medicinal preparations in pharmacies. I. Suspensions for dermal administration].[药房制剂配制标准规范。I. 皮肤给药混悬剂]
Ceska Slov Farm. 2008 Apr;57(2):55-7.
3
Bulk compounding technology.批量配药技术
Am J Hosp Pharm. 1969 Nov;26(11):650-2.
4
[Obtaining of a stable suspension of barium sulfate].[获得硫酸钡的稳定悬浮液]
Farmatsiia. 1967 Jan-Feb;16(1):26-9.
5
Parenteral formulation V: development of analytical methods for a sterile product.
Bull Parenter Drug Assoc. 1971 May-Jun;25(3):140-8.
6
The use of a comparative analysis of sedimentation and Brownian motion as a guide to suspension formulation.采用沉降和布朗运动的对比分析作为混悬液制剂的指导方法。
Pharm Acta Helv. 1970 Jan;45(1):52-9.
7
The bulk compounding of technology of liquids and semi-solids.液体和半固体技术的批量配制
Am J Hosp Pharm. 1969 Feb;26(2):70-99.
8
Drug formulation and biologic availability.药物制剂与生物利用度。
Semin Drug Treat. 1971 Sep;1(2):148-76.
9
[Volume increase coefficients for solutions and suspensions of several pharmaceutical substances].
Farm Zh. 1978 Jul-Sep(4):62-4.
10
[Manufacturing and properties of pharmaceutical spray dry products].[药物喷雾干燥产品的制造与性质]
Acta Pharm Hung. 1978 Jan;48(1):19-35.

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The effect of crystallizing and non-crystallizing cosolutes on succinate buffer crystallization and the consequent pH shift in frozen solutions.结晶和非结晶共溶质对琥珀酸盐缓冲液结晶的影响以及冷冻溶液中 pH 值的相应变化。
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Points to consider when establishing drug product specifications for parenteral microspheres.考虑在为注射用微球建立药品规格时应注意的要点。
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