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ashwini bakhade @go_66a1f0105ce38
Topical Drug Delivery: Overcoming Barriers to Effectively Treat Diseases In Industry
Topical drug delivery refers to the administration of pharmaceutical products through the skin to treat local diseases or disorders. This route of administration provides direct access to the target site of action without systemic distribution. Some key advantages of topical delivery over other routes include avoidance of first-pass metabolism, localized drug effects, and minimization of systemic side effects. However, effective topical delivery also faces several challenges related to the skin's ability to serve as a barrier.

Anatomical and Physiological Barriers of the Skin

The outermost layer of skin, the stratum corneum, acts as the body's primary barrier against external substances and pathogens. Topical Drug Delivery made up of dense layers of dead, keratin-rich cells bound together by lipid matrices. This tough, lipophilic layer makes it difficult for hydrophilic drugs to permeate. Additionally, the stratum corneum constantly sheds its outer layers, limiting drug residence time on the skin. Skin renewal occurs approximately every 4 weeks, requiring repeated application of topical products.

Below the stratum corneum lies the viable epidermis, which contains living keratinocytes and Langerhans cells. Metabolic enzymes within these cells can break down drugs, reducing their availability for absorption. Furthermore, skin continuously secretes sebum from the sebaceous glands and perspiration from the sweat glands, washing away drug molecules before they can penetrate. The thickness of the stratum corneum also varies across body sites, with thicker layers on the palms and soles posing additional resistance.

Overcoming Barriers through Formulation Strategies

Various formulation approaches have been developed to help drugs surmount the skin's barrier properties. Penetration enhancers work by temporarily altering the stratum corneum's structure to make it more permeable to drug molecules. Common enhancers include oleic acid, propylene glycol, and urea. They accomplish this via mechanisms such as increasing lipid fluidity, extraction of skin lipids, or formation of aqueous channels. Another approach is to deliver drugs in a reservoir system, where the active ingredient is contained within an occlusive matrix that hydrates the skin to assist diffusion.

Drug molecular size also influences transport across membranes, with smaller molecules exhibiting better skin permeability. Therefore, prodrug design has be
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