| Literature DB >> 27339407 |
Jatinder Kaur Mukker1, Ravi Shankar Prasad Singh2, Hartmut Derendorf3.
Abstract
Inhaled corticosteroids are used as one of the first-line drug therapy in patients with asthma. However, their long-term use is associated with various oropharyngeal and systemic side and adverse effects. Design of pro-soft drug is one of the strategies, which was adopted in the design of ciclesonide for mitigation of side effects usually observed with the use of inhaled corticosteroids. Ciclesonide, a pro-soft drug, is converted to an active metabolite desisobutyryl-ciclesonide in the lungs. The anti-inflammatory effect of desisobutyryl-ciclesonide is much higher than ciclesonide, and therefore, the local effect of the metabolite is higher with lower systemic side effects. Ciclesonide has favorable pharmacokinetic and pharmacodynamic properties as inhaled corticosteroid including low oral bioavailability, high plasma protein binding and rapid systemic clearance, high pulmonary deposition and distribution and long pulmonary residence duration. These advantageous properties make ciclesonide a very effective treatment option with low side effects. Various clinical studies support safety and efficacy of ciclesonide use in mild, moderate, and severe asthma patients.Entities:
Keywords: asthma; ciclesonide; desisobutyryl-ciclesonide; inhaled corticosteroids; pro-soft drug
Mesh:
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Year: 2016 PMID: 27339407 DOI: 10.1016/j.xphs.2016.05.004
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534