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Appropriate kinetic formulations were assessed.
The formulations were assessed on assay, dissolution, friability, weight variation and disintegration time.
Formulations were assessed for percentage transmittance, droplet size and emulsification efficacy.
The formulations were assessed for globule size (nm) (Y1) and solubility of CP in microemulsion (mg/ml) (Y2).
The most appropriate formulations were assessed for mannosylation using FTIR, XPS, SEM coupled with EDX analysis, and wettability assay, in comparison with the respective non-functionalized SLNas.
Formulations were assessed for their particle size, in-vitro drug release, Scanning electron microscopy, Differential-scanning-calorimetry and Fourier transform infra-red spectroscopy studies.
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The difference in Tmax values between the two formulations was assessed using nonparametric Wilcoxon signed rank test using SAS Enterprise guide 5.1.
Anti-nociceptive efficacy of the formulations was assessed on Wistar rats by hot plate and tail flick tests, based on the response to pain perception.
In addition, acute toxicity and tolerability of our PDMS-b-PMOXA polymersome formulations was assessed in vivo using zebrafish embryos as a vertebrate screening model.
Cellular uptake of Dox-loaded formulations was assessed in HepG2 cells using fluorescence microscopy.
The exact iron concentration of the nano-chain formulations was assessed by ICP-OES after digesting all samples with concentrated HNO3 acid.
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