1,034
Views
3
CrossRef citations to date
0
Altmetric
Editorial

Recent advances in solid dispersions and the formulation of poorly absorbed drugs

References

  • Piao H, Yang L, Wang P, et al. A preformulation study of a polymeric solid dispersion of paclitaxel prepared using a quasi-emulsion solvent diffusion method to improve the oral bioavailability in rats. Drug Dev Ind Pharm 2016;42:353–63
  • Penkina A, Semjonov K, Hakola M, et al. Towards improved solubility of poorly water-soluble drugs: cryogenic co-grinding of piroxicam with carrier polymers. Drug Dev Ind Pharm 2016;42:378–88
  • Wong PCH, Heng PWS, Chan LW. A study on the solid state characteristics of spray-congealed glyceryl dibehenate solid lipid microparticles containing ibuprofen. Drug Dev Ind Pharm 2016;42:364–77
  • Oh CM, Siow CRS, Heng PWS, Chan LW. Impact of HPMC on the physical properties of spray-congealed PEG microparticles and its swelling effect on rifampicin dissolution. Drug Dev Ind Pharm 2016;42:403–11
  • Medarevića DP, Kleinebudde P, Djuriš J, et al. Combined application of mixture experimental design and artificial neural networks in the solid dispersion development. Drug Dev Ind Pharm 2016;42:389–402
  • Lang B, Liu S, McGinity JW, Williams RO III. Effect of hydrophilic additives on the dissolution and pharmacokinetic properties of itraconazole-enteric polymer hot-melt extruded amorphous solid dispersions. Drug Dev Ind Pharm 2016;42:429–45
  • Altamimi MA, Neau SA. Use of the Flory–Huggins Theory to predict the solubility of nifedipine and sulfamethoxazole in the triblock, graft copolymer Soluplus®. Drug Dev Ind Pharm 2016;42:446-455
  • Cai C, Liu M, Li Y, et al. A silica-supported solid dispersion of bifendate using supercritical carbon dioxide method with enhanced dissolution rate and oral bioavailability. Drug Dev Ind Pharm 2016;42:412–17
  • Hamdan II, El-Sabawi D, Jalil MA. Potential interaction between zinc ions and a cyclodextrin-based diclofenac formulation. Drug Dev Ind Pharm 2016;42:418–28
  • Liu Y, Chen L, Zhou C, et al. Development and evaluation of alginate-chitosan gastric floating beads loading with oxymatrine solid dispersion. Drug Dev Ind Pharm 2016;42:456–63
  • Gao Y, Xie Y, Sun H, et al. Effect of pore size of three-dimensionally ordered macroporous chitosan-silica matrix on solubility, drug release and oral bioavailability of loaded-nimodipine. Drug Dev Ind Pharm 2016;42:464–72
  • Palem CR, Battu SK, Repka MA, Yamsani MR. Development, optimization and in vivo characterization of domperidone controlled release hot melt extruded films for buccal delivery. Drug Dev Ind Pharm 2016;42:473–84
  • Lu J, Cuellar K, Hammer NI, et al. Solid-state characterization of Felodipine-Soluplus® amorphous solid dispersions. Drug Dev Ind Pharm 2016;42:485–96
  • Mehanna M, Allam A. Formulation, physicochemical characterization and in vivo evaluation of ion sensitive metformin loaded-biopolymeric beads. Drug Dev Ind Pharm 2016;42:497–505
  • Jing B, Wang Z, Yang R, et al. Enhanced oral bioavailability of felodipine by novel solid self-microemulsifying tablets. Drug Dev Ind Pharm 2016;42:506–12

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.