Inyathelo elinye eliphezulu lokuchaneka kweMalaria Pf/Pv Test kit

Uvakalelo

I-Malaria Pf/Pv Rapid Test Device (iGazi Elipheleleyo) iye yavavanywa ngemicroscope kwiisampulu zeklinikhi.Iziphumo zibonisa ukuba ubuntununtunu beMalaria Pf/Pv Rapid Test Device (Igazi Elipheleleyo) yi>98% xa kuthelekiswa neziphumo ezifunyenwe ngemicroscope.

Ukuchaza ngokuthe ngqo

I-Malaria Pf/Pv Rapid Test Device (iGazi Elipheleleyo) isebenzisa izilwa-buhlungu ezithe ngqo kwi-Malaria Pf-specific kunye ne-P.vivax LDH antigens kwigazi elipheleleyo.Iziphumo zibonisa ukuba ubume beMalaria Pf/Pv Rapid Test Device (Igazi Elipheleleyo) ingaphezulu kwama-99.9%, xa kuthelekiswa neziphumo ezifunyenwe ngemicroscope.

Izimvo: IiSampulu zeGazi ezosulelwe yiPlasmodium falciparum (n=80).I-Plasmodium vivax (n=50) yaqukwa, kunye neesampulu ezingama-451 ezinemalariya ezingalunganga eziza kuqinisekiswa ngemicroscope.
I-Relative Sensitivity ye-Pf-specific antigens: 80/80> 99.9% (96.4%～100.0%)*
I-Relative Sensitivity ye-Pv antigens: 49/50=98.0% (89.6%～100.0%)*
Iinkcukacha Ngokuhambelanayo: 451/451>99.9% (99.3%～100.0%)*
Ukuchaneka: (49+80+451)/(50+80+451)=580/581=99.8% (99.0%～100.0%)*
* 95% iThutyana lokuzithemba

UKUSETYENZISWA OKUHLOSIWEYO

IsiXhobo soVavanyo oluKhawulezayo lwe-Malaria Pf/Pv (iGazi Elipheleleyo) luvavanyo olukhawulezayo lwe-chromatographic yokukhangela umgangatho weentlobo ezimbini ze-Plasmodium falciparum (Pf) ejikelezayo kunye ne-Plasmodium vivax(Pv) kwigazi elipheleleyo.

Inzuzo yethu

1.Umvelisi oyiNgcali, ishishini “eliphambili” elikwinqanaba lesizwe.
2.Hambisa iimpahla njengesicelo somyalelo
3.ISO13485, CE, Lungisa amaxwebhu ahlukeneyo okuthumela
4.Phendula imibuzo yabathengi kwiiyure ezingama-24