Nanocrystals for enhancement of oral bioavailability of poorly water-soluble drugs
Нанокристаллы для повышения пероральной биодоступности плохо растворимых в воде лекарственных препаратов
2014-08-27
SCID: 54.1/dsurjzzm
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dissolution enhancementdrug nanocrystalshigh-pressure homogenizationoral bioavailabilitypoorly water-soluble drugs
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Abstract (AI)
Nanocrystals, a carrier-free colloidal delivery system in nano-sized range, is an interesting approach for poorly soluble drugs. Nanocrystals provide special features including enhancement of saturation solubility, dissolution velocity and adhesiveness to surface/cell membranes. Several strategies are applied for nanocrystals production including precipitation, milling, high pressure homogenization and combination methods such as NanoEdge™, SmartCrystal and Precipitation-lyophilization-homogenization (PLH) technology. For oral administration, many publications reported useful advantages of nanocrystals to improve in vivo performances i.e. pharmacokinetics, pharmacodynamics, safety and targeted delivery which were discussed in this review. Additionally, transformation of nanocrystals to final formulations and future trends of nanocrystals were also described.
Key Findings
1
Nanocrystals are carrier-free nanoscale colloidal systems designed to enhance the oral delivery of poorly water-soluble drugs.
2
Nanocrystals improve saturation solubility, dissolution velocity, and adhesion to biological surfaces or cell membranes.
3
Precipitation, milling, high-pressure homogenization, and combined technologies such as NanoEdge™, SmartCrystal, and PLH enable nanocrystal production.
4
Published studies report improved in vivo pharmacokinetics, pharmacodynamics, safety, and targeted delivery following oral nanocrystal administration.
5
The review addresses conversion of nanocrystals into final dosage forms and emerging future trends in nanocrystal-based drug delivery.
Research Object
Nanocrystals of poorly water-soluble drugs for oral administration
Research Subject
Enhancement of oral bioavailability and in vivo performance, including pharmacokinetics, pharmacodynamics, safety, and targeted delivery
Publication Details
Publication Date
2014-08-27
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