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Type IV Collagen of Basal Lamina

Type IV collagen is a 400 nm long, network-forming collagen that acts as a barrier between the epithelial and endothelial cells. Type IV collagen  forms the backbone of the basement membrane by scaffolding with laminin, entactin, proteoglycans, and fibronectin. Apart from rendering structural support to the basement membrane, it also helps entail signaling potentials necessary for both pathological and physiological functions.
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Enteric coating derived from marine sponge collagen.

Martina Nicklas1, Wolfgang Schatton, Sascha Heinemann

  • 1KliniPharm GmbH, Frankfurt, Germany.

Drug Development and Industrial Pharmacy
|October 17, 2009
PubMed
Summary

A novel enteric coating derived from marine sponge collagen provides gastroresistance for oral medications. This sustainable coating meets regulatory standards for both pharmaceuticals and dietary supplements.

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Area of Science:

  • Pharmaceutical Technology
  • Biomaterials Science
  • Marine Biotechnology

Background:

  • Enteric coatings are crucial for oral drug delivery, protecting acid-labile or stomach-irritating compounds.
  • They ensure targeted drug release in the small intestine, enhancing therapeutic efficacy.
  • Current coatings often rely on synthetic polymers, prompting a search for natural alternatives.

Purpose of the Study:

  • To develop a novel gastroresistant delayed-release tablet coating using collagen from the marine sponge Chondrosia reniformis.
  • To assess the technical feasibility and performance of this marine-derived coating material.

Main Methods:

  • An aqueous coating dispersion was formulated using freeze-dried sponge collagen (15% w/w) as the film-forming agent.
  • Disintegration tests were performed according to European Pharmacopoeia (Ph. Eur.) standards at varying coating thicknesses.
  • Reproducibility, physical properties, and long-term stability of the coated tablets were evaluated.

Main Results:

  • A coating level of 13 mg/cm² demonstrated resistance to 0.1 M hydrochloric acid for over 2 hours.
  • Tablets disintegrated within 10 minutes in a phosphate buffer solution (pH 6.8), meeting Ph. Eur. requirements.
  • The coating process was reproducible, yielding tablets with satisfactory mechanical properties and stability for at least 6 months.

Conclusions:

  • The marine sponge collagen coating (12.9 mg/cm²) successfully meets Ph. Eur. standards for gastroresistant tablets.
  • This innovative biomaterial offers a viable, natural alternative for enteric coating applications.
  • The coating material also satisfies regulatory criteria for use in dietary supplements.