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Published on: April 10, 2015
Implants composed of digoxin and poly(ε-caprolactone): development, characterization, anti-proliferative and
Abstract:
Drug delivery systems could be applied to locally treat cervical cancer, thus preventing the drawbacks of conventional therapy. In this study, anti-proliferative and anti-angiogenic effects of digoxin incorporated into poly(ε-caprolactone) implants were evaluated, aiming at the local treatment of cervical cancer. Implants were characterized, and the in vitro release profile of digoxin was demonstrated. Anti-proliferative and anti-angiogenic activities of digoxin were investigated by using chorioallantoic membrane and human cervix carcinoma (HeLa) cells, respectively. The chemical structure of digoxin and the semi-crystalline nature of poly(ε-caprolactone) were preserved after designing implants. The hydrophobicity of drug and polymer as well as the semi-crystalline structure provided a controlled diffusion of digoxin from implants. Digoxin released from implantable devices exhibited anti-proliferative activity against HeLa cells. The anti-angiogenic effect was also shown. Finally, implants composed of digoxin and poly(ε-caprolactone) could be applied as a therapeutic alternative to treat the early stage of cervical cancer, once they were able to locally control the release of this anti-angiogenic and anti-proliferative drug, minimizing its systemic side effects and toxicity.
Insights
Poly(ε-caprolactone) implants loaded with digoxin offer a novel local treatment for cervical cancer. These implants effectively deliver digoxin, reducing tumor growth and blood vessel formation while minimizing systemic toxicity.
Area of Science:
- Biomaterials Science
- Oncology
- Pharmacology
Background:
- Conventional cervical cancer therapies often cause significant systemic side effects.
- Local drug delivery systems present a promising alternative for targeted cancer treatment.
- Digoxin exhibits anti-proliferative and anti-angiogenic properties relevant to cancer therapy.
Purpose of the Study:
- To evaluate the anti-proliferative and anti-angiogenic effects of digoxin incorporated into poly(ε-caprolactone) implants for local cervical cancer treatment.
- To assess the controlled release of digoxin from poly(ε-caprolactone) implants.
- To investigate the potential of these implants as a therapeutic alternative for early-stage cervical cancer.
Main Methods:
- Poly(ε-caprolactone) implants containing digoxin were fabricated and characterized.
- In vitro release kinetics of digoxin from the implants were determined.
- Anti-proliferative activity was assessed using human cervix carcinoma (HeLa) cells.
- Anti-angiogenic effects were evaluated using the chorioallantoic membrane assay.
Main Results:
- The chemical structure of digoxin and the semi-crystalline nature of poly(ε-caprolactone) were maintained during implant fabrication.
- The hydrophobicity of digoxin and poly(ε-caprolactone), along with the polymer's structure, facilitated controlled digoxin release.
- Digoxin released from the implants demonstrated significant anti-proliferative effects on HeLa cells.
- The implants also exhibited notable anti-angiogenic activity.
Conclusions:
- Poly(ε-caprolactone) implants effectively control the local release of digoxin.
- Digoxin-loaded implants show promising anti-cancer activity, inhibiting proliferation and angiogenesis.
- These implants represent a potential therapeutic strategy for early-stage cervical cancer, offering localized treatment with reduced systemic toxicity.
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