http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104107162-B
Outgoing Links
Predicate | Object |
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classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-522 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-06 |
filingDate | 2013-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2016-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2016-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CN-104107162-B |
titleOfInvention | A kind of micro emulsion gels pharmaceutical composition and preparation method thereof |
abstract | The present invention provides a kind of acyclovir microemulsion gel preparation, mainly utilizes oil phase, aqueous phase, surfactant and cosurfactant to prepare clear O/W type acyclovir microemulsion.Add the hydrophilic gel matrix such as carbomer, prepare acyclovir micro emulsion gel.This micro emulsion gel surface is with positive charge, particle diameter is little and uniform, particle mean size controls within 50nm, the micro-structure (hair follicle, sebaceous gland, sweat gland opening) of skin can be infiltrated through by carrying medicaments, and it is detained wherein, improve the skin hold-up of medicine, and play drug release effect in chronic skin.Compared with ordinary gel preparation, micro emulsion gels has skin targeting better and thinks use, can be used for treating the relevant diseases such as viral infection. |
priorityDate | 2013-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 357.