I-SARS-CoV-2 i-Antigen Rapid Test (i-Colloidal Gold) yenzelwe ukufunyaniswa okusemgangathweni kwe-SARS-CoV-2 Antigen(i-Nucleocapsid protein) kwisampulu ze-swab yeempumlo kwi-vitro. Iziphumo ezilungileyo zibonisa ubukho be-antigen ye-SARS-CoV-2. Kufuneka ifunyaniswe ngakumbi ngokudibanisa imbali yesigulana kunye nolunye ulwazi loxilongo[1]. Iziphumo ezilungileyo azilubandakanyi usulelo lwentsholongwane okanye olunye usulelo lwentsholongwane. Iintsholongwane ezifunyenweyo azingoyena nobangela uphambili weempawu zesifo. Iziphumo ezibi azilubandakanyi usulelo lwe-SARS-CoV-2, kwaye akufuneki ibe kuphela kwesiseko sonyango okanye izigqibo zolawulo lwesigulane (kubandakanywa nezigqibo zolawulo losulelo). Nika ingqalelo kwimbali yoqhagamshelwano yamva nje yesigulana, imbali yonyango kunye neempawu ezifanayo kunye neempawu ze-COVID-19, ukuba kuyimfuneko, kuyacetyiswa ukuba uqinisekise ezi sampuli ngovavanyo lwe-PCR lolawulo lwesigulana. Yeyabasebenzi baselabhoratri abafumene isikhokelo okanye uqeqesho lobuchwephesha. kwaye babe nolwazi lobuchwephesha lokuxilongwa kwe-in vitro, nakubasebenzi abafanelekileyo abafumene ulawulo losulelo okanye uqeqesho lobunesi[2].