Prodrugs of Theophylline Incorporating Ethyleneoxy Groups in the Promoiety: Synthesis, Characterization, and Transdermal Delivery-Reference-Cited by-同舟云学术

Prodrugs of Theophylline Incorporating Ethyleneoxy Groups in the Promoiety: Synthesis, Characterization, and Transdermal Delivery

Published:2012-05-31 Issue:3 Volume:13 Page:853-862
ISSN:1530-9932
Container-title:AAPS PharmSciTech
language:en
Short-container-title:AAPS PharmSciTech

Author:

Majumdar Susruta,Mueller-Spaeth Maren,Sloan Kenneth B.

Publisher

Springer Science and Business Media LLC

Subject

Drug Discovery,Pharmaceutical Science,Agronomy and Crop Science,Ecology,Aquatic Science,General Medicine,Ecology, Evolution, Behavior and Systematics

Link

http://link.springer.com/content/pdf/10.1208/s12249-012-9803-6.pdf

Reference31 articles.

1. Sloan KB, Bodor N. Hydroxymethyl and acyloxymethyl prodrugs of theophylline: enhanced delivery of polar drugs through skin. Int J Pharm. 1982;12:299–313.

2. Kerr D, Roberts W, Tebbett I, Sloan KB. 7-Alkylcarbonyloxymethyl prodrugs of theophylline: topical delivery of theophylline. Int J Pharm. 1998;167:37–48.

3. Sloan KB, Koch SAM, Siver KG. Mannich base derivatives of theophylline and 5-fluorouracil: Synthesis, properties and topical delivery characteristics. Int J Pharm. 1984;21:251–64.

4. Sloan KB. Functional group considerations in the development of prodrug approaches to solving topical delivery problems. In: Sloan KB, editor. Prodrugs: topical and ocular drug delivery. New York: Marcel Dekker; 1992. p. 17–116.

5. Sloan KB. Prodrugs for dermal delivery. Adv Drug Deliv Rev. 1989;3:67–101.

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