“…To overcome problems of container volumes, several devices have been applied for buffalo MII oocyte vitrification by using very small amounts of solution and submerging the sample quickly into the LN 2 (Table 6). This includes SSV (Atabay et al, 2013;Boonkusol et al, 2007;Gasparrini et al, 2007;Liang, Rakwongrit, et al, 2012), Cryoloop (Gasparrini et al, 2007), Cryotop (Atabay et al, 2013;Attanasio, Boccia, et al, 2010;Liang, Rakwongrit, et al, 2012;Muenthaisong et al, 2007;Wang et al, 2016), straws (Gautam et al, 2008), and microdrop (Liang, Srirattana, et al, 2012). Cryotop has been successfully applied for IVM oocytes and SCNT blastocysts (Laowtammathron et al, 2005;Parnpai et al, 2004Parnpai et al, , 2016.…”