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Encapsulation of Cancer Therapeutic Agent Dacarbazine Using Nanostructured Lipid Carrier
Published on: April 26, 2016
Recent advances in nano vehicles encapsulating cinnamic acid and its derivatives as promising anticancer agents
Nadine Wafik Nabih1, Mohamed S Nafie2,3, Asaad Babker4
1Organic and Medicinal Chemistry Department, Faculty of Pharmacy, University of Sadat City Sadat City Menoufia 32897 Egypt.
Abstract:
Although progress in cancer diagnosis and treatment has been substantial over recent decades, several challenges remain unresolved. Among these challenges are drug resistance, the recurrence of metastatic disease, off-target toxic effects, and nonselective drug targeting. In response, increasing attention has turned to naturally derived anticancer agents that may offer both efficacy and improved safety profiles. Among these, cinnamic acid, a phenylacrylic compound abundant in Lauraceae plants such as cinnamon, has shown remarkable antitumor activity against several cancer types. However, like many phytochemicals, its clinical utility is hampered by poor water solubility, low bioavailability, and unstable pharmacokinetics. In recent years, integrating nanotechnology into drug delivery strategies has opened new avenues for overcoming these limitations. This review explores the most recent developments in the nanoformulation of cinnamic acid and its derivatives, focusing on how nanocarriers may enhance their therapeutic potential in both in vitro and in vivo cancer models.
Insights
Cinnamic acid shows anticancer promise, but poor solubility limits its use. Nanotechnology offers a solution by improving delivery and enhancing the therapeutic potential of this natural compound in cancer treatment.
Area of Science:
- Natural Product Chemistry
- Nanotechnology
- Oncology
Background:
- Despite advances, cancer treatment faces challenges like drug resistance and toxicity.
- Naturally derived compounds, such as cinnamic acid from cinnamon, exhibit antitumor properties.
- Phytochemicals like cinnamic acid often suffer from poor solubility and bioavailability, hindering clinical application.
Purpose of the Study:
- To review recent advancements in nanoformulating cinnamic acid and its derivatives.
- To explore how nanocarriers can overcome the limitations of cinnamic acid for cancer therapy.
- To assess the enhanced therapeutic potential of nanoformulated cinnamic acid in preclinical cancer models.
Main Methods:
- Literature review of recent studies on cinnamic acid nanoformulations.
- Analysis of various nanocarrier systems used for cinnamic acid delivery.
- Evaluation of in vitro and in vivo data on the efficacy and safety of nanoformulated cinnamic acid.
Main Results:
- Various nanocarrier systems, including nanoparticles, liposomes, and micelles, have been developed for cinnamic acid.
- Nanoformulation significantly improves the solubility, bioavailability, and pharmacokinetic profile of cinnamic acid.
- In vitro and in vivo studies demonstrate enhanced anticancer activity and reduced toxicity of nanoformulated cinnamic acid compared to the free drug.
Conclusions:
- Nanoformulation is a promising strategy to enhance the clinical utility of cinnamic acid as an anticancer agent.
- Nanocarriers effectively address the delivery challenges associated with cinnamic acid, improving its therapeutic index.
- Further research into optimized nanoformulations could lead to novel and safer cancer therapies.
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