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Technically yes, but its not recommended

The shared biological properties of exendin-4 and human GLP-1 probably stem from their primary and secondary structures, but exendin-4 is naturally resistant to degradation by the DPP-4 enzyme, attributed to the presence of glycine at position 2, resulting in an intravenous half-life of approximately 30 minutes ( Figure 2 , Table 1 ], which became the first FDA-approved GLP-1RA in 2005 for the treatment of T2DM in adults [ Table 2 ]

Glutathione oxidized in this manner forms glutathione disulphide (GSSG), which is recycled back to GSH by the enzyme glutathione reductase (Glr1p)

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