Engineering a Remedy to Modulate and Optimize Biopharmaceutical Properties of Rebamipide by Synthesizing New Cocrystal: In Silico and Experimental Studies

Pharm Res. 2021 Dec;38(12):2129-2145. doi: 10.1007/s11095-021-03132-7. Epub 2021 Dec 13.

Abstract

Purpose: Rebamipide (REB) a potent anti-ulcer agent, has not been exploited to its full potential, owing to it extremely poor solubility, leading to highly diminutive bioavailability (<10%). The purpose is to carry out its solid-state modification.

Method: Cocrystallisation was done with three GRAS coformers namely citric acid (CA), 3,4-dihydroxybenzoic acid (DHBA) and oxalic acid (OXA) employing the liquid-assisted grinding method. Cocrystal formation was based upon amide-carboxyl and amide-hydroxyl supramolecular synthons. Characterization of novel cocrystals i.e. RCA, RDHBA and ROXA was carried out by DSC, PXRD and additionally by FT-IR spectroscopy. Chemical structures have been determined utilizing the PXRD pattern by Material Studio®. Furthermore, cocrystals were subjected to solubility and intrinsic dissolution rate (IDR) evaluation. Also, pharmacodynamic and pharmacokinetic studies were performed and compared with pure rebamipide.

Result: The appearances of a single sharp melting endotherm in DSC, along with novel characteristic peaks in PXRD infer the existence of a new crystalline form. Shifting in characteristic vibrations in FT-IR spectroscopy supports the establishment of distinct hydrogen-bonded networks. Structural determination revealed that RCA crystallizes in 'Bb2b' space groups whereas RDHBA in 'P1' and ROXA crystallize out in the 'P-1' space group. All the cocrystals exhibited superior apparent solubility and almost 7-13 folds increase in IDR. Furthermore, 1.6-2.5 folds enhancement in relative bioavailability and remarkable amplification in anti-ulcer, anti-inflammatory and the antioxidant potential of these cocrystals were observed.

Conclusion: The study ascertains the advantages of cocrystallization, with RCA showing greatest potential and suggests a viable alternative approach for improved formulation of rebamipide.

Keywords: Anti-inflammatory; Anti-oxidant; Anti-ulcer; Cocrystals; Rebamipide.

MeSH terms

  • Alanine / administration & dosage
  • Alanine / analogs & derivatives*
  • Alanine / chemistry
  • Alanine / pharmacokinetics
  • Animals
  • Biological Availability
  • Biological Products / chemistry*
  • Biological Products / pharmacokinetics
  • Carrageenan / administration & dosage
  • Carrageenan / immunology
  • Chemical Engineering*
  • Chemistry, Pharmaceutical / methods
  • Crystallization
  • Disease Models, Animal
  • Drug Compounding / methods
  • Edema / chemically induced
  • Edema / drug therapy*
  • Edema / immunology
  • Humans
  • Hydrogen Bonding
  • Indomethacin
  • Male
  • Powder Diffraction
  • Quinolones / administration & dosage
  • Quinolones / chemistry*
  • Quinolones / pharmacokinetics
  • Rats
  • Spectroscopy, Fourier Transform Infrared
  • Stomach Ulcer / chemically induced
  • Stomach Ulcer / drug therapy*

Substances

  • Biological Products
  • Quinolones
  • Carrageenan
  • rebamipide
  • Alanine
  • Indomethacin