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Table 1 System Suitability results of the proposed method

From: Development and validation of a stability-indicating RP-HPLC method for estimation of Lefamulin in pure and pharmaceutical drug products

System suitability parameters

Resultsa

Acceptance criteria

Retention time (tR)

3.1 ± 0.1 min

± 5% of window

Tailing factor (Tf)

1.12 ± 0.05

0.8–2.0

No. of theoretical plates (N)

5000 ± 500

≥ 2000

Peak purity index

1.0000

≥ 0.999

%RSD of peak areas

0.108%

≤ 2.0%

  1. aMean of five replicates