Literature DB >> 34071110

Achievements in Thermosensitive Gelling Systems for Rectal Administration.

Maria Bialik1, Marzena Kuras1, Marcin Sobczak1, Ewa Oledzka1.   

Abstract

Rectal drug delivery is an effective alternative to oral and parenteral treatments. This route allows for both local and systemic drug therapy. Traditional rectal dosage formulations have historically been used for localised treatments, including laxatives, hemorrhoid therapy and antipyretics. However, this form of drug dosage often feels alien and uncomfortable to a patient, encouraging refusal. The limitations of conventional solid suppositories can be overcome by creating a thermosensitive liquid suppository. Unfortunately, there are currently only a few studies describing their use in therapy. However, recent trends indicate an increase in the development of this modern therapeutic system. This review introduces a novel rectal drug delivery system with the goal of summarising recent developments in thermosensitive liquid suppositories for analgesic, anticancer, antiemetic, antihypertensive, psychiatric, antiallergic, anaesthetic, antimalarial drugs and insulin. The report also presents the impact of various types of components and their concentration on the properties of this rectal dosage form. Further research into such formulations is certainly needed in order to meet the high demand for modern, efficient rectal gelling systems. Continued research and development in this field would undoubtedly further reveal the hidden potential of rectal drug delivery systems.

Entities:  

Keywords:  drug delivery system; poloxamer; rectal drug delivery; rectal gel; solid suppository; thermosensitive gel; thermosensitive liquid suppository

Year:  2021        PMID: 34071110     DOI: 10.3390/ijms22115500

Source DB:  PubMed          Journal:  Int J Mol Sci        ISSN: 1422-0067            Impact factor:   5.923


  81 in total

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7.  Physicochemical characterization and in vivo evaluation of thermosensitive diclofenac liquid suppository.

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Journal:  Arch Pharm Res       Date:  2003-02       Impact factor: 4.946

8.  H(1) antihistamine drug promethazine directly blocks hERG K(+) channel.

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Journal:  Farmaco       Date:  2004-11
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  3 in total

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