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--- ncbi nlm nih gov pmc articles PMC7901515link springer com article 10 1007 s13346-021-01056-82 Conclusion There is tremendous interest in the use of dissolving microneedles for transdermal drug delivery This can be attributed to the fact that these devices can incorporate medications in the polymeric matrices which dissolve in the skin upon application releasing drugs which are transported into the blood --- tandfonline com doi full 10 1080 09540105 2016 1148667The aim of this study was to develop and characterize an intranasal delivery system for amantadine hydrochloride (AMT) Optimal formulations consisted of a thermosensitive polymer Pluronic® 127 and either carboxymethyl cellulose or chitosan which demonstrated gel transition at nasal cavity temperatures (34 ± 1°C) --- sciencedirect com science article abs pii S0022354915002415A novel AM hapten was prepared, and a sensitive monoclonal antibody against AM was developed The optimum ic-ELISA conditions included a pH of 7 4 and an ionic strength of 1 6% with no organic solvents The half-inhibition concentration (IC 50) value of ic-ELISA was 1 92 ng ml, with a limit of detection of 0 62 ng ml Transdermal drug delivery is a viable and clinically proven route of administration This route specifically requires overcoming the mechanical barrier provided by the Stratum Corneum of epidermis and vascular and nervous networks within the dermis First-generation Transdermal patches and second-generation iontophoretic patches have been translated into commercial clinical products --- ncbi nlm nih gov pmc articles PMC4695825--- nejm org doi full 10 1056 NEJMoa1102609--- ncbi nlm nih gov books NBK499953Interestingly, spray angles of 60 and 70 lead to deposition of the formulation in the olfactory regions of the nasal cavity, sug-gesting the possibility for exploitation in nose-to-brain delivery of amantadine FCS sprayed at an angle of 60 with insertion lead to olfactory deposition of 0 6-0 7 cm2 For FCMC, a greater olfactory deposition of 0 A more recent large-sample (n = 184) placebo-controlled RCT of amantadine involved patients 4–16 weeks after severe TBI presenting as the vegetative state or minimally conscious state demonstrated faster recovery on the DRS and Coma Recovery Scale-Revised (CRS-R) in an active-treatment group during the 4-week treatment period (Giacino et al 2012) During the 4-week treatment period, recovery was significantly faster in the amantadine group than in the placebo group, as measured by the DRS score (difference in slope, 0 24 points per week; P --- sciencedirect com science article pii S0753332217324149Amantadine inhibits the replication of influenza A virus isolates from each of the subtypes (ie, H1N1, H2N2 and H3N2), but has very little or no activity against influenza B virus isolates Parkinson disease: The exact mechanism of amantadine in the treatment of Parkinson disease and drug-induced extrapyramidal symptoms is not known --- medicine com drug amantadine hcpAmantadine is an antiviral agent with mild antiparkinsonian activity Amantadine was used in the early 2000s for Influenza A treatment However, high levels of resistance have emerged recently, initially from Asia and now in North America As of 2011, the CDC does not recommend treatment or prophylaxis of influenza A due to the high levels of resistance Amantadine is now used mostly for A stainless steel microneedle roller was used in this study to deliver the antiparkinsonian agents amantadine hydrochloride and pramipexole dihydrochloride across porcine skin The microneedle roller contains microneedles protruding from a cylindrical surface measuring 500 μm in length per microneedle with a density of 192 needles ( Figure 1 ) --- jpharmsci org article S0022-3549(15)00241-5 pdf
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