메뉴 건너뛰기




Volumn 12, Issue 2, 2011, Pages 56-61

Effective formulation development strategies for poorly soluble active pharmaceutical ingredients (APIs)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLODEXTRIN DERIVATIVE; ITRACONAZOLE; SODIUM CHLORIDE; SOLVENT; SURFACTANT;

EID: 79954996191     PISSN: 19453337     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (7)

References (28)
  • 1
    • 0034461768 scopus 로고    scopus 로고
    • Drug-like properties and the causes of poor solubility and permeability
    • Lipinski, C.A. Drug-like properties and the causes of poor solubility and permeability, J. Pharmacol. Toxicol Methods, 44: 235-249 (2000).
    • (2000) J. Pharmacol. Toxicol Methods , vol.44 , pp. 235-249
    • Lipinski, C.A.1
  • 2
  • 3
    • 78049495059 scopus 로고    scopus 로고
    • The developability classification system: Application of biopharmaceutics concepts to formulation development
    • DOI 10.1002/jps.22217
    • Butler, J.M., Dressman, J.B. The developability classification system: Application of biopharmaceutics concepts to formulation development, J. Pharm. Sci., DOI 10.1002/jps.22217 (2010).
    • (2010) J. Pharm. Sci.
    • Butler, J.M.1    Dressman, J.B.2
  • 4
    • 0028948839 scopus 로고
    • A theoretical basis for a biopharmaceutical drug classification: The correlation in vitro drug product dissolution and in vivo bioavailability
    • Amidon, G.L., Lennernas, H., Shah, V.P., Crison, J.R. A theoretical basis for a biopharmaceutical drug classification: the correlation in vitro drug product dissolution and in vivo bioavailability, Pharmaceutical Research, 12: 413-420 (1995).
    • (1995) Pharmaceutical Research , vol.12 , pp. 413-420
    • Amidon, G.L.1    Lennernas, H.2    Shah, V.P.3    Crison, J.R.4
  • 5
    • 33947487639 scopus 로고
    • The rate of solution of a solid substance in their own solutions
    • Noyes, A.A., Whitney, W.R., The rate of solution of a solid substance in their own solutions, J. Am. Chem. Soc., 19; 930 (1897).
    • (1897) J. Am. Chem. Soc. , vol.19 , pp. 930
    • Noyes, A.A.1    Whitney, W.R.2
  • 6
    • 34548032742 scopus 로고    scopus 로고
    • Salt formation to improve drug solubility
    • Serajuddin, A.T.M., Salt formation to improve drug solubility, Adv. Drug Deliv. Revs., 59; 603-616 (2007).
    • (2007) Adv. Drug Deliv. Revs. , vol.59 , pp. 603-616
    • Serajuddin, A.T.M.1
  • 9
    • 34548049483 scopus 로고    scopus 로고
    • Nanosizing - Oral formulation development and biopharmaceutical evaluation
    • Kesisoglou, F., Panmai, S., Wu, Y., Nanosizing - Oral formulation development and biopharmaceutical evaluation, Advanced Drug Delivery Reviews, 59; 631-644 (2007).
    • (2007) Advanced Drug Delivery Reviews , vol.59 , pp. 631-644
    • Kesisoglou, F.1    Panmai, S.2    Wu, Y.3
  • 10
    • 20844446627 scopus 로고    scopus 로고
    • The role of bio-pharmaceutics in the development of a clinical nanoparticle formulation of MK-0869: A beagle dog model predicts improved bioavailability and reduced food effect on absorption in humans
    • Wu, Y, Loper, A., Landis, L, Hettrick, L, Novak, L., Lynn, K., Chen, C, Thompson, K., Higgins, R., Batra, U., Shelukar, S., Kwei, g., Storey, D., The role of bio-pharmaceutics in the development of a clinical nanoparticle formulation of MK-0869: a beagle dog model predicts improved bioavailability and reduced food effect on absorption in humans, Int. J. Pharm., 285; 135-146 (2004).
    • (2004) Int. J. Pharm. , vol.285 , pp. 135-146
    • Wu, Y.1    Loper, A.2    Landis, L.3    Hettrick, L.4    Novak, L.5    Lynn, K.6    Chen, C.7    Thompson, K.8    Higgins, R.9    Batra, U.10    Shelukar, S.11    Kwei, G.12    Storey, D.13
  • 11
    • 0029023516 scopus 로고
    • The effect of particle size and shape on the surface specific dissolution rate of micronized practically insoluble drugs
    • Mosharraf, M., Nystrom, C, The effect of particle size and shape on the surface specific dissolution rate of micronized practically insoluble drugs, Int. J. Pharm., 122; 35-47, (1995).
    • (1995) Int. J. Pharm. , vol.122 , pp. 35-47
    • Mosharraf, M.1    Nystrom, C.2
  • 12
    • 0342897023 scopus 로고    scopus 로고
    • Nanosuspensions for the formulation of poorly soluble drugs. I. Preparation by a size reduction technique
    • Muller, R.H., Peters, K., Nanosuspensions for the formulation of poorly soluble drugs. I. Preparation by a size reduction technique, Int. J. Pharm., 160; 229-237 (1998).
    • (1998) Int. J. Pharm. , vol.160 , pp. 229-237
    • Muller, R.H.1    Peters, K.2
  • 13
    • 52149114196 scopus 로고    scopus 로고
    • Solubilization capabilities of some cationic, anionic, and non-ionic surfactants toward the poorly water soluble antibiotic drug erythromycin
    • Bhat, PA., Dar, A.A., Rather, G.M., Solubilization capabilities of some cationic, anionic, and non-ionic surfactants toward the poorly water soluble antibiotic drug erythromycin, J. Chem. Eng. Data, 53; 1271-1277 (2008).
    • (2008) J. Chem. Eng. Data , vol.53 , pp. 1271-1277
    • Bhat, P.A.1    Dar, A.A.2    Rather, G.M.3
  • 14
    • 78149385377 scopus 로고    scopus 로고
    • Evaluation of the impact of sodium lauryl sulphate source variability on solid oral dosage form development
    • DOI: 10.3109/03639045.2010.488647
    • Qiang, D., Gunn, J.A., Schultz, L., Li, Z. J., Evaluation of the impact of sodium lauryl sulphate source variability on solid oral dosage form development, Drug Dev. Ind. Pharm., DOI: 10.3109/03639045.2010.488647 (2010).
    • (2010) Drug Dev. Ind. Pharm.
    • Qiang, D.1    Gunn, J.A.2    Schultz, L.3    Li, Z.J.4
  • 15
    • 33748515006 scopus 로고    scopus 로고
    • Study on dissolution rate enhancement of poorly water soluble drug: Contributions of solubility enhancement and relatively low micelle diffusivity
    • Joshi, V.Y, Sawant, M.R., Study on dissolution rate enhancement of poorly water soluble drug: Contributions of solubility enhancement and relatively low micelle diffusivity J. Dispers. Sci. Technol., 27; 1141-1150 (2006).
    • (2006) J. Dispers. Sci. Technol. , vol.27 , pp. 1141-1150
    • Joshi, V.Y.1    Sawant, M.R.2
  • 16
    • 34548134498 scopus 로고    scopus 로고
    • A decision support tool for the formulation of orally active, poorly soluble compounds
    • Branchu, S., Rogueda, PG., Plumb, A.P., Cook, W.G., A decision support tool for the formulation of orally active, poorly soluble compounds, Eur. J. Pharm. Sci., 32; 128-139.
    • Eur. J. Pharm. Sci. , vol.32 , pp. 128-139
    • Branchu, S.1    Rogueda, P.G.2    Plumb, A.P.3    Cook, W.G.4
  • 17
    • 34548134519 scopus 로고    scopus 로고
    • Cyclodextrins as pharmaceutical solubilizers
    • Brewster, M.E., Loftsson, T, Cyclodextrins as pharmaceutical solubilizers, J. Pharm. Sci., 59; 645-666 (2007).
    • (2007) J. Pharm. Sci. , vol.59 , pp. 645-666
    • Brewster, M.E.1    Loftsson, T.2
  • 18
    • 74049133227 scopus 로고    scopus 로고
    • Cycodextrins as solubilizers: Formation of complex aggregates
    • DOI: 10.1002/jps.21.861
    • Jansook, P., Kurkov, S.V., Loftsson, T, Cycodextrins as solubilizers: Formation of complex aggregates, J. Pharm. Sci.: DOI: 10.1002/jps.21.861 (2010).
    • (2010) J. Pharm. Sci.
    • Jansook, P.1    Kurkov, S.V.2    Loftsson, T.3
  • 19
    • 77955982703 scopus 로고    scopus 로고
    • Enhancement of the aqueous solubility and masking the bitter taste of famotidine/SBE-ß-CyD/Povidone K30 Complexation Approach
    • DOI: 10.1002/jps. 22153
    • Mady F.M., Abou-Taleb, A.E., Khaled, K.A., Yamasaki, K., Iohara, D., Ishiguro, T., Hirayama, F., Uekama, K., Otagiri, M., Enhancement of the aqueous solubility and masking the bitter taste of famotidine/SBE-ß-CyD/Povidone K30 Complexation Approach, J. Pharm. Sci., DOI: 10.1002/jps. 22153 (2010).
    • (2010) J. Pharm. Sci.
    • Mady, F.M.1    Abou-Taleb, A.E.2    Khaled, K.A.3    Yamasaki, K.4    Iohara, D.5    Ishiguro, T.6    Hirayama, F.7    Uekama, K.8    Otagiri, M.9
  • 20
    • 77951590174 scopus 로고    scopus 로고
    • The solubility-permeability interplay in using cyclodextrins as pharmaceutical solubilizers: Mechanistic modelling and application to progesterone
    • DOI: 10.1002/jps.22033
    • Dahan, A., Miller, J.M., Hoffman, A., Amidon, G.E., Amidon, G.L., The solubility-permeability interplay in using cyclodextrins as pharmaceutical solubilizers: mechanistic modelling and application to progesterone, J. Pharm. Sci., DOI: 10.1002/jps.22033 (2009).
    • (2009) J. Pharm. Sci.
    • Dahan, A.1    Miller, J.M.2    Hoffman, A.3    Amidon, G.E.4    Amidon, G.L.5
  • 21
    • 39149126301 scopus 로고    scopus 로고
    • Biopharmaceutical challenges associated with drugs with low aqueous solubility - The potential impact of lipid-based formulations
    • O'Driscoll, CM., Griffin, B.T., Biopharmaceutical challenges associated with drugs with low aqueous solubility - The potential impact of lipid-based formulations, Advanced Drug Delivery Reviews, 60; 617-624 (2008).
    • (2008) Advanced Drug Delivery Reviews , vol.60 , pp. 617-624
    • O'Driscoll, C.M.1    Griffin, B.T.2
  • 22
    • 27644444751 scopus 로고    scopus 로고
    • A quantitative approach to probe the dependence and correlation of food-effect with aqueous solubility, dose/solubility ratio, and partition coefficient (log P) for orally active drugs administered as immediate release formulations
    • Singh, B.N., A quantitative approach to probe the dependence and correlation of food-effect with aqueous solubility, dose/solubility ratio, and partition coefficient (log P) for orally active drugs administered as immediate release formulations, Drug Dev. Res., 65; 55-75 (2005).
    • (2005) Drug Dev. Res. , vol.65 , pp. 55-75
    • Singh, B.N.1
  • 24
    • 77957335795 scopus 로고    scopus 로고
    • Soft gelatin capsules (softgels)
    • DOI: 10.1002/jps.22151
    • Gullapalli, R.P., Soft gelatin capsules (softgels), J. Pharm. Sci., DOI: 10.1002/jps.22151 (2010).
    • (2010) J. Pharm. Sci.
    • Gullapalli, R.P.1
  • 25
    • 0027248233 scopus 로고
    • Chemical stability of indomethacin in the solid amorphous and molten states
    • Carstensen, J.T., Morris, T.,Chemical stability of indomethacin in the solid amorphous and molten states,J. Pharm. Sci., 82; 657 (1993).
    • (1993) J. Pharm. Sci. , vol.82 , pp. 657
    • Carstensen, J.T.1    Morris, T.2
  • 26
    • 1842865536 scopus 로고    scopus 로고
    • Melt extrusion: From process to drug delivery
    • Breitenbach, J., Melt extrusion: from process to drug delivery, Eur. J. Pharm. Biopharm., 54; 107-117 (2002).
    • (2002) Eur. J. Pharm. Biopharm. , vol.54 , pp. 107-117
    • Breitenbach, J.1
  • 27
    • 33750804217 scopus 로고    scopus 로고
    • Particle engineering techniques for inhaled biopharmaceuticals
    • Shoyele, S.A., Cawthorne, S., Particle engineering techniques for inhaled biopharmaceuticals, Advanced Drug Delivery Reviews, 58; 1009-1029 (2006).
    • (2006) Advanced Drug Delivery Reviews , vol.58 , pp. 1009-1029
    • Shoyele, S.A.1    Cawthorne, S.2
  • 28
    • 64649088132 scopus 로고    scopus 로고
    • Amorphous compositions using concentrating enhancing polymers for improved bioavailability of itraconazole
    • DiNunzio, J.C., Miller, D.A., Yang, W., McGinty, J.W., Williams, R.O., Amorphous compositions using concentrating enhancing polymers for improved bioavailability of itraconazole, Mol. Pharm., 5; 968-980 (2008).
    • (2008) Mol. Pharm. , vol.5 , pp. 968-980
    • Dinunzio, J.C.1    Miller, D.A.2    Yang, W.3    McGinty, J.W.4    Williams, R.O.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.