An intravenous formulation decision tree for discovery compound formulation development

被引:55
|
作者
Lee, YC [1 ]
Zocharski, PD [1 ]
Samas, B [1 ]
机构
[1] Pfizer Global Res & Dev, Pharmaceut Sci, Ann Arbor, MI 48105 USA
关键词
solubility; decision tree; high throughput; discovery;
D O I
10.1016/S0378-5173(02)00704-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Discovery and pre-clinical animal efficacy assessment formulation development efforts are challenged by limited compound availability and stringent timelines. The implementation and use of a systematic discovery formulation scheme can facilitate this important process. We observed that nearly 85% of Pfizer, Ann Arbor discovery compounds (n > 300) submitted for discovery and pre-clinical injectable formulation development in the year 2000 could be formulated by pH adjustment, cosolvent addition, or a combination of the two approaches. Based on the vehicle data generated by this laboratory, a discovery formulation decision tree, that utilizes the solubilization approaches described above, is proposed. The proposed decision tree can be adapted and modified by pharmaceutical scientists to conform to best practices put forth by their institutions for discovery animal studies requiring injectable dosage forms. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:111 / 119
页数:9
相关论文
共 50 条
  • [1] Clinical Development of Ganaxolone as an Intravenous Formulation
    Lappalainen, Jaakko
    Saporito, Michael
    NEUROTHERAPEUTICS, 2016, 13 (03) : 649 - 649
  • [2] Preformulation and formulation development of a bioactive nitroaromatic compound
    Camila F. A. Sena
    Lívia S. Apolinário
    Jaqueline A. Duarte
    Giovanna C. dos Santos
    Liziane O. F. Monteiro
    Mônica C. de Oliveira
    Elaine A. Leite
    Renata B. de Oliveira
    Journal of Nanoparticle Research, 2017, 19
  • [3] Preformulation and formulation development of a bioactive nitroaromatic compound
    Sena, Camila F. A.
    Apolinario, Livia S.
    Duarte, Jaqueline A.
    dos Santos, Giovanna C.
    Monteiro, Liziane O. F.
    de Oliveira, Monica C.
    Leite, Elaine A.
    de Oliveira, Renata B.
    JOURNAL OF NANOPARTICLE RESEARCH, 2017, 19 (11)
  • [4] Drug discovery and formulation development for acute pancreatitis
    Jiang, Xue
    Zheng, Ya-Wen
    Bao, Shihui
    Zhang, Hailin
    Chen, Ruijie
    Yao, Qing
    Kou, Longfa
    DRUG DELIVERY, 2020, 27 (01) : 1562 - 1580
  • [5] Product development of fenretinide, NSC 374551, intravenous formulation
    Gupta, S
    Zgodinski, J
    Vishnuvajjala, R
    Solomon, D
    EUROPEAN JOURNAL OF CANCER, 2002, 38 : S21 - S21
  • [6] Formulation in Drug Discovery
    Strickley, Robert G.
    ANNUAL REPORTS IN MEDICINAL CHEMISTRY, VOL 43, 2008, 43 : 419 - 451
  • [7] Development of a copper-clioquinol formulation suitable for intravenous use
    Wehbe, Moe
    Malhotra, Armaan K.
    Anantha, Malathi
    Lo, Cody
    Dragowska, Wieslawa H.
    Dos Santos, Nancy
    Bally, Marcel B.
    DRUG DELIVERY AND TRANSLATIONAL RESEARCH, 2018, 8 (01) : 239 - 251
  • [8] Development of a copper-clioquinol formulation suitable for intravenous use
    Moe Wehbe
    Armaan K. Malhotra
    Malathi Anantha
    Cody Lo
    Wieslawa H. Dragowska
    Nancy Dos Santos
    Marcel B. Bally
    Drug Delivery and Translational Research, 2018, 8 : 239 - 251
  • [9] Formulation aspects of intravenous nanosuspensions
    Patel, Dipeekakumari
    Zode, Sandeep S.
    Bansal, Arvind K.
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2020, 586
  • [10] Safety of an intravenous formulation of lamotrigine
    Conway, Jeannine M.
    Birnbaum, Angela K.
    Leppik, Ilo E.
    Pennell, Page B.
    White, James R.
    Rarick, John O.
    Remmel, Rory P.
    SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2014, 23 (05): : 390 - 392