Electrospinning-based wound dressings
with multifunctional properties,
including hemostasis-promoting, antibacterial, drug release, and therapeutic
effects, are of great interest in military and civilian trauma healthcare.
Herein, we designed lidocaine hydrochloride (LID) and mupirocin-loaded
chitosan/polycaprolactone (CSLD-PCLM) scaffolds with multiple functions
as wound dressings. Through the dual spinneret electrospinning technique,
the scaffolds achieved a nanofiber structure, which enhanced the interfacial
interaction between the scaffold and blood cells and showed excellent
blood coagulation capacity. In particular, the scaffolds loaded with
LID and mupirocin exhibited rapid release of LID and sustained release
of mupirocin. The CSLD-PCLM scaffold containing mupirocin exhibited
outstanding antibacterial activity. Moreover, the scaffold significantly
enhanced the wound healing process with complete re-epithelialization
as well as collagen deposition in a full-thickness skin defect model.
Thus, CSLD-PCLM nanofibrous scaffolds may ideally meet the various
requirements of the wound healing process and are promising candidates
for wound dressings in future clinical applications.
Cancer immunotherapy is a promising approach that has recently gained its importance in treating cancer. Despite various approaches of immunotherapies being used to target cancer cells, they are either not effective against all types of cancer or for all patients. Although efforts are being made to improve the cancer immunotherapy in all possible ways, one important hindrance that lowers the immune response to kill cancer cells is the infiltration of Regulatory T (Treg) cells into the tumor cells, favoring tumor progression, on one hand, and inhibiting the activation of T cells to respond to cancer cells, on the other hand. Therefore, new anti-cancer drugs and vaccines fail to show promising results against cancer. This is due to the infiltration of Treg cells into the tumor region and suppression of anti-cancer activity. Thus, regardless of various types of immunotherapies being practiced, understanding the mechanisms of how Treg cells favor tumor progression and inhibition of anti-cancer activity is worthwhile. Therefore, the review highlights the importance of Tregs cells and how depletion of Treg cells can pave the way to an effective immunotherapy by activating the immune responses against cancer.
A piperazine oligomer (PE) has been successfully synthesized via green and facile conditions. To obtain equivalent or better antimicrobial activity and smaller cytotoxicity, a mechano-growth factor and its 24-amino acid peptide analog corresponding to the unique C-terminal E-domain (MGF-Ct24E) was introduced to the side chain of PE. Fourier transform infrared spectrometry (FTIR), elemental analysis, and amino acid analyzer (AAA) measurements showed that the MGF-Ct24E-modified piperazine polymer (PEM) was successfully prepared. The antibacterial activity and cytotoxicity of PEM were further investigated. Introduction of MGF-Ct24E resulted in equivalent or improved antibacterial properties and reduced cytotoxicity compared to PE. The resulting material may replenish the current arsenal of synthetic polymeric antibacterial systems reported.
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