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Bratisl Lek Listy ; 125(7): 435-7440, 2024.
Article in English | MEDLINE | ID: mdl-38943505

ABSTRACT

OBJECTIVES: To create a new mucoadhesive dosage form based on PluronicF127 followed by transformation into a gel form upon intranasal administration for targeted delivery to brain tissueMETHODS: Citicoline, cytidine diphosphocholine, designated as CDP-choline, was purchased as a white powder with the molecular weight of 510.31 g/mol. The triblock copolymers of polyethylene glycol-block-polypropylene glycol-block-polyethylene glycol (PEG-PPG-PEG), branded as Pluronic F127, was used. RESULTS: When instilled into the nasal cavity, Pluronic F127 for intranasal administration is transformed into a gel that remains retained for 45-55 minutes, which promotes better penetration of drugs into the brain tissue. CONCLUSION: The polymer's gelling and adhesive properties performed well, which is crucial for further research at the preclinical stage (Tab. 1, Fig. 5, Ref. 28).


Subject(s)
Administration, Intranasal , Brain , Drug Delivery Systems , Poloxamer , Poloxamer/administration & dosage , Brain/metabolism , Animals , Cytidine Diphosphate Choline/administration & dosage , Cytidine Diphosphate Choline/pharmacokinetics , Gels , Polyethylene Glycols/administration & dosage , Polyethylene Glycols/pharmacokinetics , Nasal Mucosa/metabolism
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