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Citation: Fc. Pennie et al., A longitudinal study of the biometric and refractive changes in full-term infants during the first year of life, VISION RES, 41(21), 2001, pp. 2799-2810
Authors:
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Citation: Sm. Khoo et al., A conscious dog model for assessing the absorption, enterocyte-based metabolism, and intestinal lymphatic transport of halofantrine, J PHARM SCI, 90(10), 2001, pp. 1599-1607
Citation: Cjh. Porter et Wn. Charman, Lipid-based formulations for oral administration - Opportunities for bioavailability enhancement and lipoprotein targeting of lipophilic drugs, DRUG PHARM, 115, 2001, pp. 85-130
Citation: Sm. Khoo et al., The formulation of Halofantrine as either non-solubilising PEG 6000 or solubilising lipid based solid dispersions: Physical stability and absolute bioavailability assessment, INT J PHARM, 205(1-2), 2000, pp. 65-78
Authors:
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Charman, WN
Miller, R
Porter, CJH
Citation: Kc. Lyons et al., Factors limiting the oral bioavailability of N-acetylglucosaminyl-N-acetylmuramyl dipeptide (GMDP) and enhancement of absorption in rats by delivery in a water-in-oil microemulsion, INT J PHARM, 199(1), 2000, pp. 17-28
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