Results 251 to 260 of about 177,103 (312)
A biomimetic hydrogel derived from neonatal spinal cord ECM (DNSCM) delivers LAMB2 protein and ISP peptide to remodel the inhibitory injury microenvironment. The system sustains drug release, upregulates pro‐regenerative LAMB2, downregulates inhibitory CSPG, and promotes axonal regeneration.
Shiyu Fu +8 more
wiley +1 more source
Thioketal (TK) polymers are promising biomaterials due to their selective biodegradation by reactive oxygen species (ROS), but they respond slowly to physiologic doses of ROS. Here, the TK bond's pendant groups are modified to enhance the degradation of TK‐based implants both in vitro and in vivo.
Karina A. Bruce +6 more
wiley +1 more source
Mesoblends consist of a nanostructured polymer into which a second polymer is imbibed with a selective solvent. In this work, a solvent‐templatable pentablock terpolymer possessing a sulfonated midblock is modified with a hydrophilic polymer that is photocrosslinked in situ, yielding a hierarchical binetwork.
Kacie M. Wells +3 more
wiley +1 more source
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Microneedles with Tunable Dissolution Rate
ACS Biomaterials Science & Engineering, 2020Dissolvable microneedle (MN) patches have been widely investigated for transdermal drug delivery. The dissolution rate of MN controls the status of drug release from the MN, which in turn determines drug absorption through skin. However, no systematic approaches have been reported to tune the dissolution profile of dissolvable MN matrices.
Himanshu Kathuria +4 more
openaire +2 more sources
Dissolution Rate Equations in CoIumn-Confined Dissolution
Journal of Pharmaceutical Sciences, 1976Equations are derived for the dissolution of a soluble solid in a column into a liquid stream. The equations are substantiated by experiments using oxalic acid dihydrate as a test substance. The dissolution rate constant, k, of oxalic acid dihydrate depends on linear velocity, v (centimeters per second), by the following equation: k = (2.54 +/- 0.76) X
J T, Carstensen, K, Dhupar
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Dissolution Rates of Polyphase Mixtures
Journal of Pharmaceutical Sciences, 1965The theory for the dissolution rate of polyphase mixtures has been investigated and applied to several situations. Physical models involving simultaneous diffusion and rapid equilibria have led to relationships that describe experimental data rather well for the benzoic acid–salicylic acid, the benzocaine–caffeine, and the benzoic acid–trisodium ...
W I, Higuchi, N A, Mir, S J, Desai
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Dissolution rates of silicate cements
Biomaterials, 1982The literature relating to the dissolution of the silicate cements is reviewed, including the methodology, intrinsic factors relating to composition and method of mixing, curing etc. and extrinsic factors, i.e. the medium, pH, ionic strength etc. to which the sample of cement is exposed.
A T, Kuhn, G B, Winter, W K, Tan
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Nonsink Dissolution Rate Equations
Journal of Pharmaceutical Sciences, 1975In spite of the fact that film theory is based on severe assumptionss, it is shown to be a good working model. The Niebergall-Goyan equation, the Short-Sharkey-Rhodes equation, and the Pothisiri-Carstensen equation-all based on simple film theory-are shown to hold through 80-90% of the dissolutin process for p-hydroxybenzoic acid and sodium chloride ...
M, Patel, J T, Carstensen
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Nonsink Dissolution Rate Equation
Journal of Pharmaceutical Sciences, 1973An equation was developed which describes the dissolution of monodisperse particles beyond the point where concentrations are small compared to solubility. If it is assumed that a stagnant layer model applies, the thickness of these layers is of the same order of magnitude as calculated via the Hixson-Crowell treatment but dissolution rate constants ...
P, Pothisiri, J T, Carstensen
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Controlled Release with Finite Dissolution Rate
SIAM Journal on Applied Mathematics, 2011We consider a two-phase generalization of the classical Higuchi model for controlled drug release. The drug is assumed to be prepared in a stent in its solid phase by immersion in a polymeric matrix, which eventually delivers the drug when it reaches the free end.
BISCARI, PAOLO +4 more
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