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Table 14 Optimized formulation of conventional and pH-sensitive formulation

From: Preparation and in vitro evaluation of BBG-250 loaded liposomal formulation for anticancer potential

Formulation code

Lipid ratio

Drug (mg)

Sonication time

Particle size (nm)

PDI

Entrapment efficiency

Zeta potential

P1

3:2:3:0.3

4

4 min

325 ± 1.6

0.230

49%

 − 53

P2

3:3:3:0.3

4

4 min

370 ± 0.2

0.165

52%

 − 55

P3

3:4:3:0.3

4

4 min

390 ± 1.3

0.599

75%

 − 37

P4

4:2:3:0.3

4

4 min

156 ± 1.4

0.230

72%

 − 20

P5

4:3:3:0.3

4

4 min

118 ± 1.2

0.165

78%

 − 25

P6

4:4:3:0.3

4

4 min

290 ± 0.8

0.599

65%

 − 47

P7

5:2:3:0.3

4

4 min

328 ± 0.6

0.230

69%

 − 30

P8

5:3:3:0.3

4

4 min

425 ± 1.2

0.165

70%

 − 22

P9

5:4:3:0.3

4

4 min

609 ± 0.6

0.599

45%

 − 41

P10

8:2:0.3

4

4 min

425 ± 0.6

0.215

35

 − 59

P11

7:3:0.3

4

4 min

125 ± 0.3

0.316

64

 − 28

P12

6:4:0.3

4

4 min

356 ± 0.9

0.366

52

 − 38

  1. Lipid Ratio P1-P9 (DPPC: DOPE: Cholesterol: DSPE-PEG2000); P10-P12 (HSPC: Cholesterol: DSPE-PEG2000)
  2. Bold letters highlight the highest drug release in both formulations, whether HSPC or pH-sensitive