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1.
Langmuir ; 40(37): 19766-19774, 2024 Sep 17.
Article in English | MEDLINE | ID: mdl-39235374

ABSTRACT

High blood glucose and insufficient angiogenesis in diabetic wounds prevent healing, often leading to amputation or death. To address this, a multifunctional emulsion loaded with simvastatin and stabilized by enzymes was synthesized using ultrasound-assisted emulsification. This emulsion promotes angiogenesis and reduces blood glucose levels. Glucose oxidase and catalase at the emulsion interface catalyze a glucose cascading response, lowering the glucose concentration at the diabetic wound site and improving the wound microenvironment. Simvastatin in the emulsion further promotes angiogenesis. The emulsion significantly accelerated wound healing in diabetic rats, offering a promising approach to diabetic wound management.


Subject(s)
Diabetes Mellitus, Experimental , Emulsions , Glucose Oxidase , Wound Healing , Animals , Emulsions/chemistry , Wound Healing/drug effects , Rats , Diabetes Mellitus, Experimental/drug therapy , Glucose Oxidase/chemistry , Glucose Oxidase/metabolism , Simvastatin/chemistry , Simvastatin/pharmacology , Catalase/chemistry , Catalase/metabolism , Oxygen/chemistry , Blood Glucose/drug effects , Rats, Sprague-Dawley
2.
ACS Appl Mater Interfaces ; 16(21): 27988-27997, 2024 May 29.
Article in English | MEDLINE | ID: mdl-38748900

ABSTRACT

Pickering emulsions stabilized by functional nanoparticles (NPs) have received considerable attention for improving the physical stability and biological function of NPs. Herein, hydrophobic polyphenols were chosen as phenolic ligands to form metal-phenolic network (MPN) coatings on NPs (e.g., silica, polystyrene) mediated by the sono-Fenton reaction. The MPN coatings modulated the surface wettability and charges of NPs and achieved emulsification behavior for preparing Pickering emulsions with pH responsiveness and oxidation resistance. A series of polyphenols, including resveratrol, rutin, naringin, and curcumin, were used to form MPN coatings on NPs, which served as stabilizers for the engineering of functionalized oil-in-water (O/W) Pickering emulsions. This work provides a new avenue for the use of hydrophobic polyphenols to modulate NP emulsifiers, which broadens the application of polyphenols for constructing Pickering emulsions with antioxidant properties.

3.
Biomacromolecules ; 24(11): 5394-5402, 2023 11 13.
Article in English | MEDLINE | ID: mdl-37870194

ABSTRACT

Intrinsic hemostasis is an innate body response to prevent bleeding based on the sol-gel transition of blood. However, it is often inadequate for exceptional situations, such as acute injury and coagulation disorders, which typically require immediate medical intervention. Herein, we report the preparation of an efficient hemostatic powder, composed of tannic acid (TA), poly(ethylene glycol) (PEG), and poly(d,l-lactide-co-glycolide)-b-poly(ethylene glycol)-b-poly(d,l-lactide-co-glycolide) triblock copolymer (TB), for biomimetic hemostasis at the bleeding sites. TA has a high affinity for biomolecules and cells and can form coacervates with PEG driven by hydrogen bonding. TB enhances the mechanical strength and provides thermoresponsiveness. The hemostatic powder can rapidly transit into a physical and biodegradable seal on wet substrates under physiological conditions, demonstrating its promise for the generation of instant artificial clots. Importantly, this process is independent of the innate blood clotting process, which could benefit those with blood clotting disorders. This biomimetic hemostatic powder is an adaptive topical sealing agent for noncompressible and irregular wounds, which is promising for biomedical applications.


Subject(s)
Biomimetics , Hemostatics , Powders , Polylactic Acid-Polyglycolic Acid Copolymer , Polymers , Polyethylene Glycols/chemistry , Hemostatics/pharmacology
4.
Biomacromolecules ; 24(11): 5303-5312, 2023 11 13.
Article in English | MEDLINE | ID: mdl-37748036

ABSTRACT

Bleeding after venipuncture could cause blood loss, hematoma, bruising, hemorrhagic shock, and even death. Herein, a hemostatic needle with antibacterial property is developed via coating of biologically derived carboxymethyl chitosan (CMCS) and Cirsium setosum extract (CsE). The rapid transition from films of the coatings to hydrogels under a wet environment provides an opportunity to detach the coatings from needles and subsequently seal the punctured site. The hydrogels do not significantly influence the healing process of the puncture site. After hemostasis, the coatings on hemostatic needles degrade in 72 h without inducing a systemic immune response. The composition of CMCS can inhibit bacteria of Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus by destroying the membrane of bacteria. The hemostatic needle with good hemostasis efficacy, antibacterial property, and safety is promising for the prevention of bleeding-associated complications in practical applications.


Subject(s)
Chitosan , Hemostatics , Hemostatics/pharmacology , Anti-Bacterial Agents/pharmacology , Hemostasis , Hydrogels/pharmacology , Chitosan/pharmacology , Staphylococcus aureus
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