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Enhanced chartreusin solubility by hydroxybenzoate hydrotropy.

G K Poochikian, J C Cradock

Journal of Pharmaceutical Sciences

|June 1, 1979

Summary

Hydroxybenzoates significantly enhance the aqueous solubility of the cytotoxic agent chartreusin. This solubility increase, particularly at neutral pH, is attributed to micellization, aiding drug delivery.

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Enhanced chartreusin solubility by hydroxybenzoate hydrotropy.

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Uridine-induced hyperthermia in the rabbit.

Tricyclo[4.2.2.0(2,5)]dec-9-ene-3,4,7,8-tetracarboxylic acid diimide: formulation and stability studies.

Disposition and bioavailability of various formulations of tetrahydrocannabinol in the rhesus monkey.

Related Experiment Videos

Enhanced chartreusin solubility by hydroxybenzoate hydrotropy.

Related Concept Videos

Related Articles

Arabinosyl-5-azacytosine: a novel nucleoside entering clinical trials.

Stability of cisplatin, iproplatin, carboplatin, and tetraplatin in commonly used intravenous solutions.

Therapeutic and pharmacokinetic relationships of flavone acetic acid: an agent with activity against solid tumors.

Uridine-induced hyperthermia in the rabbit.

Tricyclo[4.2.2.0(2,5)]dec-9-ene-3,4,7,8-tetracarboxylic acid diimide: formulation and stability studies.

Disposition and bioavailability of various formulations of tetrahydrocannabinol in the rhesus monkey.

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