Article
Thermosetting gels with modulated gelation temperature for ophthalmic use: the rheological and gamma scintigraphic studies.
School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Journal of Controlled Release (impact factor:
5.73).
10/2002;
83(1):65-74.
DOI:10.1016/S0168-3659(02)00175-X
pp.65-74
Source: PubMed
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Citations (0)
- Cited In (6)
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Article: Thermosensitive Self-Assembling Block Copolymers as Drug Delivery Systems
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ABSTRACT: Self-assembling block copolymers (poloxamers, PEG/PLA and PEG/PLGA diblock and triblock copolymers, PEG/polycaprolactone, polyether modified poly(Acrylic Acid)) with large solubility difference between hydrophilic and hydrophobic moieties have the property of forming temperature dependent micellar aggregates and, after a further temperature increase, of gellifying due to micelle aggregation or packing. This property enables drugs to be mixed in the sol state at room temperature then the solution can be injected into a target tissue, forming a gel depot in-situ at body temperature with the goal of providing drug release control. The presence of micellar structures that give rise to thermoreversible gels, characterized by low toxicity and mucomimetic properties, makes this delivery system capable of solubilizing water-insoluble or poorly soluble drugs and of protecting labile molecules such as proteins and peptide drugs.Polymers. 01/2011; 3:779-811. -
Article: Part II: Enhancement of transcorneal delivery of gatifloxacin by solid lipid nanoparticles in comparison to commercial aqueous eye drops.
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ABSTRACT: This study describes corneal permeation of gatifloxacin from solid lipid nanoparticle (SLN) through the cornea and its effect on corneal hydration level. The aqueous humor levels of gatifloxacin after single topical instillation in Gate(®) Eyedrops and positively charged SLN-C were determined. A 3.37-fold increase in the relative bioavailability was observed with the SLN-C (AUC(0→∞) 2.192 μg mL(-1) h) (AUC, area under the curve) as compared to Gate(®) Eyedrops (AUC(0→∞) 0.651 μg mL(-1) h). The t(1/2) of drug in SLN-C exhibited a 2.34-fold higher than Gate(®) Eyedrops seem to be significantly increased (p > 0.05), C(max) of gatifloxacin from SLN-C showed 1.09-fold higher concentration as compared to Gate(®) Eyedrops. The results suggested that SLNs could enhance ocular bioavailability of gatifloxacin and prolong its residence time in the eyes. Moreover, no signs of ocular irritation were seen with the SLN formulations, indicating their relative safety compared to the marketed drops. © 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2012.Journal of Biomedical Materials Research Part A 11/2012; · 2.63 Impact Factor -
Article: NOVEL PARADIGMS IN MUCOADHESIVE DRUG DELIVERY
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ABSTRACT: Mucoadhesion is a field of current interest in the design of drug delivery systems. Mucoadhesion is commonly defined as the adhesion between two materials, at least one of which is a mucosal surface. Mucoadhesive drug delivery system may be designed to enable prolonged residence time of the dosage form at the site of application or absorption and facilitate an intimate contact of the dosage form with the underline absorption surface. Extending the residence time of a dosage form at a particular site and controlling the release of drug from the dosage form are useful especially for achieving controlled plasma level of the drug as well as improving bioavailability. Application of these dosage forms to mucosal surfaces may be of benefit to drug molecules not amenable to the oral route, such as those that undergo acid degradation or extensive first-pass metabolism. The present review describes mucoadhesion, mucoadhesive polymers and use of these polymers in designing different types of mucoadhesive gastrointestinal, nasal, ocular, vaginal and rectal drug delivery systems. The research on mucoadhesives, however, is still in its early stage, and further advances need to be made for the successful translation of the concept into practical application in controlled drug delivery.International Journal of Pharmaceutical Sciences and Research (IJPSR). 07/2012; 3(8):2455-2471.
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Keywords
25 degrees C
combined Pluronic formulation
corneal residence time
decreased gel strength
Dynamic rheological method
elasticity modulus
firm gel
incorporating mucoadhesive polysaccharide
individual 21% F127 solution
ophthalmic drug delivery
phase transition temperature
Pluronic F127 solutions
Pluronic solutions
poor topical bioavailability
sensitive ocular tissues
sodium hyaluronate
suitable phase transition temperature
tear dilution
thermosetting gel
thermosetting gels