Abstract:Mesoporous materials bear great potential for biotechnological applications due to their biocompatibility and versatility. Their high surface area and pore interconnection allow the immobilization of molecules and their subsequent controlled delivery. Modifications of the mesoporous material with the addition of different chemical species, make them particularly suitable for the production of bioactive coatings. Functionalized thin films of mesoporous silica and titania can be used as scaffolds with properties… Show more
“…Moreover, compared with the no-heat group, the mild heat treatment group showed better and earlier recovery from the wound. Therefore, it can be concluded that mild temperature can stimulate the tissue to undergo the first stage of the repair process [ 28 , 37 , 38 , 39 ]. The results also demonstrated that the drug-loaded PP film significantly impacted the dermal healing process, and this effect was improved using remote mild heating.…”
The development of externally controlled drug delivery systems that can rapidly trigger drug release is widely expected to change the landscape of future drug carriers. In this study, a drug delivery system was developed for on-demand therapeutic effects. The thermoresponsive paraffin film can be loaded on the basis of therapeutic need, including local anesthetic (lidocaine) or topical antibiotic (neomycin), controlled remotely by a portable mini-heater. The application of mild temperature (45 °C) to the drug-loaded paraffin film allowed a rapid stimulus response within a short time (5 min). This system exploits regular drug release and the rapid generation of mild heat to trigger a burst release of 80% within 6 h of any locally administered drug. The in vitro drug release studies and in vivo therapeutic activity were observed for local anesthesia and wound healing using a neomycin-loaded film. The studies demonstrated on-demand drug release with minimized inflammation and microbial infection. This temperature-responsive drug-loaded film can be triggered remotely to provide flexible control of dose magnitude and timing. Our preclinical studies on these remotely adjustable drug delivery systems can significantly improve patient compliance and medical practice.
“…Moreover, compared with the no-heat group, the mild heat treatment group showed better and earlier recovery from the wound. Therefore, it can be concluded that mild temperature can stimulate the tissue to undergo the first stage of the repair process [ 28 , 37 , 38 , 39 ]. The results also demonstrated that the drug-loaded PP film significantly impacted the dermal healing process, and this effect was improved using remote mild heating.…”
The development of externally controlled drug delivery systems that can rapidly trigger drug release is widely expected to change the landscape of future drug carriers. In this study, a drug delivery system was developed for on-demand therapeutic effects. The thermoresponsive paraffin film can be loaded on the basis of therapeutic need, including local anesthetic (lidocaine) or topical antibiotic (neomycin), controlled remotely by a portable mini-heater. The application of mild temperature (45 °C) to the drug-loaded paraffin film allowed a rapid stimulus response within a short time (5 min). This system exploits regular drug release and the rapid generation of mild heat to trigger a burst release of 80% within 6 h of any locally administered drug. The in vitro drug release studies and in vivo therapeutic activity were observed for local anesthesia and wound healing using a neomycin-loaded film. The studies demonstrated on-demand drug release with minimized inflammation and microbial infection. This temperature-responsive drug-loaded film can be triggered remotely to provide flexible control of dose magnitude and timing. Our preclinical studies on these remotely adjustable drug delivery systems can significantly improve patient compliance and medical practice.
“… 58 For example, antibacterial agents incorporated mesoporous titania thin films characterized by controlled drug release, high pore volume and high surface area which make them ideal drug loading site is among the promising materials which can be coated onto the medical devices. 59 Atefyekta et al reported titanium oxide-based mesoporous titania thin film loaded with the antimicrobial agents (vancomycin, gentamicin, and daptomycin) in its pore volume. The thin film is characterized by decreased biofilm attachment to its surface and tunable antibacterial loading observed to be increased with increasing pore volume; thus highly contribute to host tissue growth and reduced biomaterial associated infections.…”
Antimicrobial thin films are types of protective coatings that are applied to surfaces such as medical devices, food packaging materials, water treatment membranes, water-resistant coatings, and other systems.
“…[ 5 ] Among other materials, modified porous support materials are suitable for high‐throughput applications due to their high specific surface area allowing high loading densities of active components. [ 6 ] Mesoporous inorganic and organic–inorganic hybrid films haveattracted growing interest due to their versatile potential in biotechnological applications, [ 7 ] electrochemical energy storage and conversion, [ 8 ] catalysis [ 9 ] as well as sensing. [ 10 ] Fabrication of mesoporous silica films is in most cases based on Evaporation‐Induced Self‐Assembly (EISA).…”
Combinatorial sensing is especially important in the context of modern drug development to enable fast screening of large data sets. Mesoporous silica materials offer high surface area and a wide range of functionalization possibilities. By adding structural control, the combination of structural and functional control along all length scales opens a new pathway that permits larger amounts of analytes being tested simultaneously for complex sensing tasks. This study presents a fast and simple way to produce mesoporous silica in various shapes and sizes between 0.27–6 mm by using light‐induced sol‐gel chemistry and digital light processing (DLP). Shape‐selective functionalization of mesoporous silica is successfully carried out either after printing using organosilanes or in situ while printing through the use of functional mesopore template for the in situ functionalization approach. Shape‐selective adsorption of dyes is shown as a demonstrator toward shape selective screening of potential analytes.
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