70560-51-9 Purity
95%
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Specification
Wang, Zhiwei, et al. Regenerative Biomaterials 11 (2024): rbae024.
This study used sucrose octasulfate potassium salt (hereafter PSO) as the active agent in a porous double-network hydrogel designed by a high internal phase emulsion (HIPE) approach. The PSO-loaded p(MMA-co-AM)/PVA@PSO hydrogel combined an interconnected polyHIPE architecture, strong mechanical integrity, and high drug-loading/release capability. In vitro and in vivo evaluations showed that the hydrogel system provided biocompatible, sustained delivery of PSO and promoted multiple healing endpoints in diabetic wounds (reduced MMP-9 activity, enhanced angiogenesis and growth factor secretion, increased collagen deposition, and accelerated re-epithelialization).
Preparation method and procedure:
· HIPE technique: The continuous polymer phase was formed via a high internal phase emulsion to create a polyHIPE microstructure-resulting in an interconnected porous morphology with high porosity and large specific surface area.
· PSO incorporation: PSO was added to the dispersed (internal) phase during the initial synthesis stage to produce p(MMA-co-AM)/PVA@PSO hydrogels with varying PSO loading. The reported PSO loadings tested were in the range 0.1-0.5 g (added during the first phase of synthesis).
· Processing details: PVA (0.8 g) was dissolved in deionized water with stirring at 80 °C. Monomers (MMA, AM), crosslinker (DVB), initiator (potassium persulfate), surfactant (Span80) and water were combined following the study's formulation proportions. The mixture was polymerized at 60 °C to form the HIPE prepolymer, then subjected to freezing at -20 °C for 6 hours and thawing at 25 °C for 2 hours. The hydrogel network was established by repeating freeze-thaw cycles five times.
Passali, Desiderio, et al. SpringerPlus 2.1 (2013): 668.
Nasal obstruction is one of the most frequent symptoms of upper respiratory diseases. Its treatment at the level of symptomatic supportive therapy is reduced to washing procedures. The aim of the study was to determine the clinical effectiveness of the hypertonic nasal solution containing silver sucrose octasulfate (IASOS) and potassium sucrose octasulfate (KSOS) in the treatment of patients with moderate severity of persistent nasal obstruction. The composition of the test solution is due to the synergistic effect of the antimicrobial action of IASOS and carbohydrate-induced microbial anti-adhesion and mucosal trophic properties of KSOS.
Methodology: A clinical study was conducted with 55 patients (aged 25-70) suffering from obstructive rhinopathy with persistent nasal congestion. Participants were randomly assigned to use either the hypertonic solution or an isotonic solution for 20 days. Assessments were performed at baseline (T0), day 10 (T10), and day 20 (T20).
Key Results:
· The AAR analysis demonstrated that the SILSOS group experienced a statistically significant (p<0.05) improvement in expiratory nasal airflow at both T10 and T20 compared to baseline.
· Mucociliary Clearance: While no significant change in mucociliary transport time (MCTt) was observed, the mean Mucociliary Clearance (MCC) values showed significant improvement by T20.
· Symptomatic Relief: The total VAS score indicated progressive improvement throughout the entire treatment period.
· The therapeutic benefit was sustained post-treatment. At the 30-day follow-up, only 3 patients from the hypertonic solution group reported a return of nasal obstruction, which was mild in form.
The molecular formula of sucrose octasulfate potassium salt is C12H14K8O35S8.
Some synonyms for sucrose octasulfate potassium salt are potassium sucrose octasulfate, Sucrosofate potassium anhydrous, and Sucrose octasulphate potassium salt.
The CAS number for sucrose octasulfate potassium salt is 73264-44-5.
The IUPAC name of sucrose octasulfate potassium salt is octapotassium;[(2R,3R,4S,5R,6R)-2-[(2S,3S,4R,5R)-3,4-disulfonatooxy-2,5-bis(sulfonatooxymethyl)oxolan-2-yl]oxy-3,5-disulfonatooxy-6-(sulfonatooxymethyl)oxan-4-yl] sulfate.
The InChI key of sucrose octasulfate potassium salt is XISWAUUBQBEDFB-QRDGSJRXSA-F.
There are 8 potassium ions present in sucrose octasulfate potassium salt.
The EC number of sucrose octasulfate potassium salt is 615-946-5.
The computed SMILES notation for sucrose octasulfate potassium salt is C(C1C(C(C(C(O1)OC2(C(C(C(O2)COS(=O)(=O)[O-])OS(=O)(=O)[O-])OS(=O)(=O)[O-])COS(=O)(=O)[O-])OS(=O)(=O)[O-])OS(=O)(=O)[O-])OS(=O)(=O)[O-])OS(=O)(=O)[O-].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].
The computed InChI of sucrose octasulfate potassium salt is InChI=1S/C12H22O35S8.8K/c13-48(14,15)37-1-4-6(43-51(22,23)24)8(45-53(28,29)30)9(46-54(31,32)33)11(40-4)42-12(3-39-50(19,20)21)10(47-55(34,35)36)7(44-52(25,26)27)5(41-12)2-38-49(16,17)18;;;;;;;;/h4-11H,1-3H2,(H,13,14,15)(H,16,17,18)(H,19,20,21)(H,22,23,24)(H,25,26,27)(H,28,29,30)(H,31,32,33)(H,34,35,36);;;;;;;;/q;8*+1/p-8/t4-,5-,6-,7-,8+,9-,10+,11-,12+;;;;;;;;/m1......../s1.
The modify date of sucrose octasulfate potassium salt is 2023-08-26.
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