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Related Concept Videos

Bioavailability Enhancement: Drug Permeability Enhancement01:27

Bioavailability Enhancement: Drug Permeability Enhancement

After oral administration, poor permeability often limits the rate at which drugs are absorbed through the intestinal epithelium. Enhancing drug permeability is crucial for effective therapy, and several strategies have been developed to overcome this challenge.One effective strategy involves the use of lipid-based formulations. These formulations enhance dissolution and solubility, targeting physiological mechanisms to increase drug absorption. This includes stimulating bile salt secretion,...
Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence01:27

Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence

Changes in polymorphic forms can significantly influence the bioavailability of poorly soluble drugs. Although the FDA defines pharmaceutical equivalence based on having the same active ingredient, dosage form, and route of administration, it does not automatically disqualify products with different polymorphic forms. This means two products with different polymorphs can still be deemed pharmaceutically equivalent. However, polymorphic differences can affect properties like wettability,...

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Updated: May 29, 2026

Testing the In Vitro and In Vivo Efficiency of mRNA-Lipid Nanoparticles Formulated by Microfluidic Mixing
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Lipoplatin formulation review article.

G P Stathopoulos1, T Boulikas

  • 1First Oncology Clinic, Errikos Dunant Hospital, Athens, Greece.

Journal of Drug Delivery
|September 10, 2011
PubMed
Summary
This summary is machine-generated.

Lipoplatin, a novel liposomal encapsulation of cisplatin, demonstrates superior efficacy and reduced side effects compared to traditional cisplatin in non-squamous non-small-cell lung cancer clinical trials.

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Area of Science:

  • Oncology
  • Nanotechnology
  • Pharmaceutical Sciences

Background:

  • Cisplatin is a cornerstone chemotherapy agent, but its efficacy is limited by significant toxicity.
  • Liposomal encapsulation offers a strategy to improve drug delivery and reduce side effects.
  • Lipoplatin utilizes patented technology for targeted delivery of cisplatin via nanoparticles.

Purpose of the Study:

  • To review the molecular mechanisms, preclinical, and clinical data of Lipoplatin.
  • To evaluate Lipoplatin's efficacy and safety profile in various cancer types.
  • To assess Lipoplatin's potential to replace or enhance cisplatin therapy.

Main Methods:

  • Review of published preclinical and clinical trial data.
  • Analysis of molecular mechanisms of liposomal cisplatin.
  • Examination of data from three randomized Phase II and III clinical trials.

Main Results:

  • Lipoplatin has been successfully administered in multiple clinical trials.
  • Clinical data primarily focuses on non-small-cell lung cancer, with additional data in pancreatic, breast, and head and neck cancers.
  • A Phase III study showed Lipoplatin's superiority over cisplatin in non-squamous non-small-cell lung cancer, with simultaneous reduction in side effects.

Conclusions:

  • Lipoplatin represents a significant advancement in platinum-based chemotherapy.
  • Lipoplatin demonstrates improved efficacy and a better safety profile than cisplatin.
  • Lipoplatin is expected to expand therapeutic applications and potentially replace cisplatin.