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每一經除菌過濾之卡格林肽(cagrilintide)和司馬魯肽(semaglutide)配方，均填充入雙室玻璃注射器中(請參見圖1)，以使每一注射器在朝向針頭之遠端室內含有至少500 µl可抽取體積之司馬魯肽(semaglutide)配方之一，以及於近端室內含有至少250 µl可抽取體積之卡格林肽(cagrilintide)配方，該近端室以兩個氯化丁基橡膠栓塞密封。因此，在雙室注射器中獲得總計四種不同的司馬魯肽(semaglutide)和卡格林肽(cagrilintide)配方組合。每一組合皆進行範例3中詳細描述的“噴射實驗”，並使用MFI設備和軟體獲得尺寸＞10 µm和尺寸＞25 µm(ECD)的各顆粒數量(標準化為每毫升分析液體的計數)。Each of the cagrilintide and semaglutide formulations that have been sterilized and filtered are filled into a dual-chamber glass syringe (see Figure 1), so that each syringe contains at least One of 500 µl extractable volume of semaglutide formula, and at least 250 µl extractable volume of cagrilintide formula in the proximal chamber, which is plugged with two chlorinated butyl rubbers seal