Pharmacokinetic Comparison of Once-Daily Topical Minocycline Foam 4% vs Oral Minocycline for Moderate-to-Severe Acne.

Author: EllmanHerman, JonesTerry M, deVriesTina

Paper Details 
Original Abstract of the Article :
To characterize minocycline pharmacokinetics and relative bioavailability following multiple-dose topical administration of minocycline hydrochloride (HCl) foam 4% (FMX101 4%) as compared with single-dose oral administration of minocycline HCl extended-release tablets (Solodyn®) in subjects with mod...See full text at original site
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引用元:
https://pubmed.ncbi.nlm.nih.gov/29036256

データ提供:米国国立医学図書館(NLM)

Topical Minocycline: A Skin-Deep Approach

The field of [dermatology] is constantly seeking [effective and well-tolerated] treatments for [skin conditions]. This study compares the [pharmacokinetics] of [topical minocycline foam 4%] to [oral minocycline] in [patients with moderate-to-severe acne]. The authors investigated the [absorption and bioavailability] of the topical formulation and found that it achieved [comparable plasma concentrations] to the oral formulation, suggesting that [topical minocycline] could be a viable alternative for managing [acne].

Topical Minocycline: A Promising Alternative

This study found that [topical minocycline foam 4%] was [effective] in achieving [comparable plasma concentrations] to [oral minocycline], offering a potential alternative for managing [acne] with a [less invasive] approach.

Treating Acne: Exploring New Options

This research highlights the [potential benefits] of [topical minocycline] as a [treatment option] for [acne]. It provides valuable information for [dermatologists] and [patients] seeking [effective and well-tolerated] treatments for this common skin condition.

Dr.Camel's Conclusion

Acne can feel like a desert landscape on your skin – rough, bumpy, and sometimes difficult to manage. This research offers a potential oasis in the form of [topical minocycline], providing a new avenue for treating acne with a more targeted approach.

Date :
  1. Date Completed 2018-05-29
  2. Date Revised 2018-05-29
Further Info :

Pubmed ID

29036256

DOI: Digital Object Identifier

S1545961617P1022X

Related Literature

SNS
PICO Info
in preparation
Languages

English

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