• Patchless Transdermal Drug Delivery ... - Ecn5.com ecn5
• Patchless Transdermal Drug Delivery ... - Ecn5.com ecn5
• Patchless Transdermal Drug Delivery ... - Ecn5.com ecn5
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10<br />
MARCH 2011 <strong>•</strong> TransDermal<br />
philic, it also helps to moisturize the skin, an added<br />
benefit.<br />
PharmaDur film on the skin serves as a matrix for<br />
the drug and other nonvolatile excipients for the<br />
product formulation. The skin retains the polymer<br />
film and the drug contained therein for 24+ hours,<br />
and the film provides continuous release of the drug<br />
by a process of diffusion for transdermal delivery to<br />
the body (Figure 2). The formed polymer film is not<br />
removed by perspiration or articles of clothing or<br />
transferred by touch. Thus, it functions as a virtual<br />
patch without the limitations of plastic patches.<br />
Formation of an invisible hydrogel patch for time<br />
release of medications is an attractive concept for the<br />
Figure 2<br />
Schematic Diagram of PharmaDur Virtual<br />
Patch on Skin<br />
Figure 3<br />
Comparison of Flux of Caffeine with Oleic Acid<br />
Formulations (controls) and with Added 2%<br />
PharmaDur Polymer<br />
consumer. A cosmetically elegant and invisible virtual<br />
patch is a unique concept for transdermal delivery<br />
of drugs, such as nonsteroidal, anti-inflammatory<br />
drugs (NSAIDs) for systemic activity. The<br />
virtual patch provides the following key advantages:<br />
<strong>•</strong> Delivers drugs requiring a high dosage or those<br />
with low skin permeability effectively since<br />
patients can apply the product over a large area of<br />
skin (~ 300 to 500 cm2).<br />
<strong>•</strong> Provides all-day, sustained therapeutic efficacy<br />
with a once-a-day application due to its long-lasting<br />
retention on skin, which also improves convenience<br />
for and compliance by consumers.<br />
<strong>•</strong> Reduces undesirable side effects due to avoidance<br />
of peaks and valleys in systemic drug concentrations<br />
as are typically found with oral drug<br />
administration.<br />
<strong>•</strong> Delivers many drugs that are not suitable for<br />
transdermal administration using conventional<br />
plastic patches and semisolid dosage forms.<br />
Furthermore, our studies have shown that the Pharma<br />
Dur polymer acts synergistically with skin-penetration<br />
enhancers in maximizing the rate of transdermal<br />
drug delivery. For example, Michniak et al<br />
(28) previously reported the effect of PharmaDur<br />
polymer on transdermal permeation of caffeine in<br />
the presence of the enhancer oleic acid. The re -<br />
searchers studied the skin-permeation rate of caffeine<br />
with and without the PharmaDur polymer,<br />
using human cadaver skin and Franz diffusion cells.<br />
The presence of the PharmaDur polymer almost<br />
doubled the skin-permeation rate of caffeine compared<br />
to that of the control formulation consisting of<br />
caffeine and oleic acid (Figure 3).<br />
The researchers postulate that the PharmaDur polymer<br />
film provides controlled release of both caffeine<br />
and the enhancer, thereby maximizing the enhancement<br />
in the caffeine permeation rate.<br />
Conclusion<br />
<strong>Patchless</strong> TDD is emerging as a convenient and<br />
patient-friendly means for extending the scope of<br />
transdermal delivery of drugs. Several new products<br />
and technologies using this approach for eliciting<br />
both local and systemic therapeutic effects have<br />
emerged in the last decade.