Table 7 Statistical comparison of the results obtained by applying the proposed HPLC method and the reported one13 in spiked human plasma, for determination of SAC and VAL in (a) their pure forms, and in (b) pharmaceutical dosage forms.

From: A sensitive green HPLC-fluorescence method for simultaneous analysis of sacubitril and valsartan in pure forms, pharmaceutical dosage form and human plasma

Parameter

SAC

VAL

Proposed method

Reported method*

Proposed method

Reported method*

(a)

 Mean

100.18

100.10

100.40

99.24

 SD

1.33

0.91

1.00

0.48

 Variance

1.77

0.83

1.00

0.23

 n

5

5

5

5

 Student’s t-test (2.306)**

0.103

1.642

 F value (5.32)**

2.12

4.34

(b)

 Mean

101.46

101.08

102.84

100.59

 SD

0.18

0.36

0.91

1.67

 Variance

0.03

0.13

0.83

2.79

 n

3

3

3

3

 Student’s t-test (2.776)**

1.744

2.045

 F value (7.71)**

3.85

3.37

  1. *HPLC method carried out on C18 column (15 cm) using water with 0.1% triethylamine (pH 3.5 with phosphoric acid), methanol and ethanol (30:40:30, v/v) as a mobile phase and a UV detector at wavelength of 267 nm.
  2. **Figures in parenthesis are the corresponding tabulated values at P = 0.05.