1.Use biologic fibrin adhesive in otologic surgery: compared with ammonium sulfate fibrin adhesive and tissell®.
Hyung Chul LEE ; Mi Gyeung YANG ; Mun Heum PARK
Yeungnam University Journal of Medicine 1991;8(1):127-135
Successful middle ear surgery requires the availability of al safe, effective bonding material. Side effect caused by synthetic materials have led to the use of biologic adhesive, However, they carry the risk of transmission of infectious diseases if they are prepared from pooled human blood. The adhesive strength of ammonium sulfate fibrin adhesive produce an adhesive strength that is half that of the homologous commercial product. It is, however, good enough for use in several otolaryngological operations, tympanoplasty, facial nerve repair, reconstruction of ossicles. Reconstruction of posterior wall of ear canal and obliteration of frontal sinus and mastoid antrum using bone dust.
Adhesives
;
Ammonium Compounds*
;
Ammonium Sulfate*
;
Communicable Diseases
;
Dust
;
Ear Canal
;
Ear, Middle
;
Facial Nerve
;
Fibrin Tissue Adhesive*
;
Fibrin*
;
Frontal Sinus
;
Humans
;
Mastoid
;
Tympanoplasty
2.Conbined approach for large tumor of cerebellopontine angle.
Jang Su SUH ; Sung Hyung LEE ; Seong Ho BAE ; Jin Kyu PARK ; Mi Gyeung YANG ; Oh Lyong KIM
Korean Journal of Otolaryngology - Head and Neck Surgery 1992;35(5):709-716
No abstract available.
Cerebellopontine Angle*
3.Inhibitory effects of surface-grafted polylactide-co-glycolide nanoparticles on the pro-inflammatory polarization of macrophages
Sang Hoon CHOI ; Gyeung Mi SEON ; Quang Canh VO ; Gitae SON ; Hyeong-Cheol YANG
Korean Journal of Dental Materials 2022;49(4):141-152
Phosphatidylserine (PS) mimics the anti-inflammatory effect of apoptotic cells by binding to the PS receptor of macrophages. In this study, the effect of PS-modified polylactide-co-glycolide (PLGA) nanoparticles on macrophage polarization was investigated.PLGA nanoparticles (PLGAnPs) containing phosphatidylcholine (PC) and PS were prepared using the emulsificationsolvent-evaporation (ESE) technique and classified as follows: 1) PC 100% (PCnP); 2) PS:PC = 50:50 (PSPCnP); and 3) PS 100% (PSnP). PS-grafted PLGAnPs tended to inhibit LPS-induced morphological change into M1 macrophages and mRNA expression of the M1 markers (TNF-α, IL-1β, IL-6, IL-12p40, CD86, and iNOS). In particular, the expressions of TNF-α, IL-6, and IL-12p40 were significantly decreased in the PSPCnP group, as compared to those of the positive control and and PLGAnP groups (p<0.05). Therefore, the study results demonstrate the potential of PS-grafted PLGAnPs in attenuating inflammation and modulating the drug delivery system.