Parenteral formulation and thermal degradation pathways of a potent rebeccamycin based indolocarbazole topoisomerase I inhibitor

Author:

Sato Yuichi,Breslin David,Kitada Hideyuki,Minagawa Wataru,Nomoto Takashi,Qin Xue-Zhi,Karki Shyam B.

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference13 articles.

1. Breslin, D., Sato, Y., Karki, S.B., in press. Mechanism of hydrolysis of a novel indolocarbazole topoisomerase I inhibitor. Eur. J. Pharm. Sci.

2. Therapeutic activity of the topoisomerase I inhibitor J-107088 [6-N-(1-hydroxymethyla-2-hydroxy)ethylamino-12,13-dihydro-13-(β-d-gluco pyranosyl)-5H-indolo[2,3-a]pyrrolo[3,4-c]-carbazole-5,7(6H)-dione] against pediatric and adult central nervous system tumor xenografts;Cavazos;Cancer Chemother. Pharmacol.,2001

3. Solubilization of NSC-639829;Jain;Int. J. Pharm.,2001

4. Excipients and their use in injectable products;Nema;PDA J. Pharm. Sci. Technol.,1997

5. Solubilization and preformulation of carbendazim;Ni;Int. J. Pharm.,2002

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