Iindaba ezimnandi!I-Shanghai Chuangkun Biotech i-15 enobungozi obuphezulu be-HPV yeekhithi zokuvavanya i-nucleic acid (i-lyophilized, indlela ye-PCR fluorescence probe), ifumene isatifikethi sobhaliso se-FDA yase-Indonesia!

Kutsha nje, iShanghai Chuangkun Biotech HPV(15 High-risk subtype) DNA PCR ukubona ikiti (lyophilized) ifumene isatifikethi sobhaliso se-FDA yase-Indonesia, ephawula ukuba iimveliso zeChuangkun Biotech ziye zamkelwa yi-FDA yase-Indonesia, ibonelela ngakumbi ngenkxaso eyomeleleyo kwi-Chuangkun Biotech ephuhlisayo. imarike yehlabathi.

Ngokwezibalo zoMbutho wezeMpilo weHlabathi, ngonyaka ka-2020, umhlaza womlomo wesibeleko kwihlabathi, izehlo zomhlaza womlomo wesibeleko phakathi kwamathumba abulalayo abasetyhini abekwe kwindawo yesine emva komhlaza wemiphunga, umhlaza wamabele kunye nomhlaza webala.Ehlabathini lonke, malunga nama-500,000 abasetyhini ababa nomhlaza womlomo wesibeleko nyaka ngamnye kwaye malunga nama-200,000 abulawa sesi sifo.Umhlaza womlomo wesibeleko kuphela kwesifo esibuhlungu se-etiology eyaziwayo phakathi kwezinto ezinobungozi zomntu.Usulelo lwe-Human papillomavirus (HPV) lubonakaliswe njengoyena nobangela womhlaza womlomo wesibeleko kunye nezilonda zawo zangaphambili (i-cervical intraepithelial neoplasia (CIN), ene-HPV16 kunye ne-18 iindidi ezinegalelo elingaphezulu kwe-50% yomhlaza womlomo wesibeleko. , Umbutho wezeMpilo weHlabathi (i-WHO) uqalise i-Global Strategy to Accelerate Elimination of Cervical Cancer, igxininisa ukubaluleka kokuhlolwa kwe-HPV. NgoJulayi 6, i-2021, i-WHO yahlaziywa kwaye yakhupha izikhokelo zokuhlola kunye nokunyangwa kwezilonda ze-cervical precancerous kumlomo wesibeleko. uthintelo lomhlaza, ukucebisa umngcipheko ophezulu we-papillomavirus yabantu (umngcipheko ophezulu we-HPV) uvavanyo lwe-DNA njengendlela ekhethwayo yokuhlola umhlaza womlomo wesibeleko.

I-Chuangkun Biotech HPV (12+3) Ikhithi yokufumanisa i-PCR ye-DNA (i-lyophilized) isekwe kwi-multiplex ye-PCR-fluorescent probe technology kwaye ifanelekile kwisixhobo se-PCR esine-channel ezine.Imveliso ithatha inkqubo yemveliso yonke icandelo lyophilization, kwaye ikiti ingathuthwa kwaye igcinwe kwiqondo lobushushu, nto leyo isombulula intlungu chain uthutho reagents ulwelo eqhelekileyo, kwaye kunokunciphisa kakhulu amalungiselelo kunye neendleko zothutho yokuthengisa phesheya.Le mveliso isetyenziselwa ukufumanisa i-in vitro ye-papillomavirus yabantu kwiiseli ezigqithisiweyo zomlomo wesibeleko, ezigubungela iintlobo ze-15 ezinobungozi obuphezulu, kwaye inokuchonga i-subtypes ezintathu ze-16, i-18 kunye ne-52. ), ukucaciswa okuphezulu, ukufakwa okuphezulu kunye nokulawulwa komgangatho wereferensi yangaphakathi, kwaye yamkela itekhnoloji yolwandiso oluthe ngqo olungatsalwanga kwaye isebenzisana neChuangkun Biotech Thunder series ekhawulezayo yesixhobo sokubona isixhobo sePCR ukugqibezela ukufunyanwa ngokukhawuleza kweesampulu eziyi-16 ~ 96 kwimizuzu engama-40, kunye iziphumo zichanekile kwaye zithembekile.

Ukufunyanwa kwesatifikethi sokubhaliswa kwe-FDA yase-Indonesia kukuqondwa ngokupheleleyo kunye nokuqinisekiswa kweemveliso zeChuangkun Biotech.Kwixesha elizayo, siya kuqhubeka nokubambelela kwintengiso-ejolise kwintengiso, inzululwazi kunye nokuveliswa kwezinto ezintsha zobuchwepheshe njengenkxaso, siphucula rhoqo ukhuphiswano olungundoqo lwamashishini, kunye nombono wehlabathi wokwakha iibrendi ezinenzuzo, ngemizamo engagungqiyo kunye nokuzingisa, ukukhuthaza uphuhliso. yeshishini lezempilo, ukufezekisa iphupha lempilo yabantu kwaye sizame nzima!