Preformulation studies to aid in the development of a ready-to-use injectable solution of the antitumor agent, topotecan

被引:14
作者
Kearney, AS
Patel, K
Palepu, NR
机构
[1] Pharmaceutical Development, SmithKline Beecham Pharmaceuticals, King of Prussia, PA 19406, 709 Swedeland Road
关键词
topotecan; anticancer; solubility; stability; deamination;
D O I
10.1016/0378-5173(95)04218-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Topotecan ((S)-9-dimethylaminomethyl-10-hydroxycamptothecin hydrochloride; SKF-S-104864-A) is a promising anticancer agent that is currently available as a lyophilized formulation. To evaluate the feasibility of formulating topotecan as a ready-to-use injectable solution, the pH-solubility profile was generated over a pH range of 2.5 to 4.5 at 25 degrees C, and the pH-stability profile was generated over a pH range of 2 to 4, a temperature range of 60-80 degrees C; and at an ionic strength of similar to 0.15 M. The former experiments revealed that desirable solubilities (i.e. 2.5 mg/ml in free base equivalents) are achievable at pH < 4, whereas extrapolation of the degradation kinetics to 25 degrees C indicated that desirable stabilities (i.e. less than or equal to 2% degradation of topotecan over 2 years) are achievable at pH < 3. The stability results are consistent with a degradation mechanism involving deamination of topotecan proceeding through a reactive quinone methide intermediate. Subsequent attack of water on this intermediate gives the dihydroxylated product, 9-hydroxymethyl-10-hydroxycamptothecin, which may then lose formaldehyde to form the monohydroxylated product, 10-hydroxycamptothecin. The overall study results suggest that a solution pH of less than or equal to 2.5 is most appropriate for the formulation of a ready-to-use solution. Prototype formulations meeting these criteria have been placed on long-term stability.
引用
收藏
页码:229 / 237
页数:9
相关论文
共 18 条
[1]  
AKIMOTO K, 1994, CHEM PHARM BULL, V42, P2135, DOI 10.1248/cpb.42.2135
[2]  
ALBERT A, 1971, IONIZATION CONSTANTS, P9
[3]   REACTIVITY OF MANNICH BASES .13. MECHANISM OF REACTION BETWEEN AMINOMETHYLNAPHTHOLS AND BENZENETHIOLS [J].
ANDRISAN.R ;
DELLACAS.C ;
TRAMONTI.M .
JOURNAL OF THE CHEMICAL SOCIETY C-ORGANIC, 1970, (13) :1866-&
[4]   ACTIVITY OF TOPOTECAN, A NEW TOPOISOMERASE-I INHIBITOR, AGAINST HUMAN TUMOR COLONY-FORMING-UNITS INVITRO [J].
BURRIS, HA ;
HANAUSKE, AR ;
JOHNSON, RK ;
MARSHALL, MH ;
KUHN, JG ;
HILSENBECK, SG ;
VONHOFF, DD .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1992, 84 (23) :1816-1820
[5]   A KINETIC AND MECHANISTIC STUDY OF THE HYDROLYSIS OF CAMPTOTHECIN AND SOME ANALOGS [J].
FASSBERG, J ;
STELLA, VJ .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1992, 81 (07) :676-684
[6]   REACTION OF PHENOLIC MANNICH BASE METHIODIDES AND OXIDES WITH VARIOUS NUCLEOPHILES [J].
GARDNER, PD ;
RAFSANJANI, HS ;
RAND, L .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1959, 81 (13) :3364-3367
[7]   EVALUATION OF 9-DIMETHYLAMINOMETHYL-10-HYDROXYCAMPTOTHECIN AGAINST XENOGRAFTS DERIVED FROM ADULT AND CHILDHOOD SOLID TUMORS [J].
HOUGHTON, PJ ;
CHESHIRE, PJ ;
MYERS, L ;
STEWART, CF ;
SYNOLD, TW ;
HOUGHTON, JA .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1992, 31 (03) :229-239
[8]  
HSIANG YH, 1989, CANCER RES, V49, P5077
[9]  
HSIANG YH, 1985, J BIOL CHEM, V260, P4873
[10]  
IVANOV BE, 1968, IAN SSSR KH, P768