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Table 5 Different analytical methods for the determination of NMV and RIT in different matrices

From: Sustainable and technically smart spectrophotometric determination of PAXLOVID: a comprehensive ecological and analytical performance rating

Method

Sample Type

Injection volume

Stationary phase

Mobile phase/ Solvent

Linearity range μg/mL

LOQ μg/mL

Detector

Refs.

Spectrophotometry

Tablets

EtOH

10–250

NMV

1D 4.14

2D 8.04

DWZ8.14

UV

This work

RIT

1D 9.75

2D 7.35

DWZ8.35

TLC-DAD

Tablets and spiked human plasma

10 µL

TLC aluminum silica gel plates

A: MeOH

B: H2O

C: 2% urea solution of β-cyclodextrin (40:10:0.5)

1–5

NMV 0.21

RIT 0.13

215 nm

[14]

HPLC–DAD

Tablets

20 µL

C18 column (4.6 × 250 mm, 5 μm particle size)

A: 20% Water

B: 80% EtOH

Flow rate: 1 mL/min

Run time 10 min

1–20

NMV 0.6

RIT 0.96

215 nm

[15]

CE-DAD

Tablets and in presence of degradation products

Inject at 50 mbar pressure, for 17 s

silica capillary (50 cm effective length × 50 μm id)

50 mM borate buffer pH 9.2 with 25 mM sodium lauryl sulfate

Run time 7 min

NMV 10–200

RIT 5–100

NMV 2.78

RIT 1.95

210 nm

[16]

HPLC–DAD

Tablets and in presence of degradation products

20 µL

C18 (4.6 × 250 mm, 5 μm particle size)

A: 50% 50 mM ammonium acetate buffer at pH 5

B: 50% ACN

Flow rate: 1 mL/min

Run time 7 min

NMV 10–200

RIT 5–100

NMV 2.22

RIT 1.23

210 nm

[16]

UPLC-MS/MS

Human plasma

5 µL

BDS Hypersil C18 column (4.6 × 100 mm, 2.4 μm)

Gradient elution

A: 0.1% formic acid H2O

B: 0.1% formic acid MeOH

Flow rate: 0.8 mL/min

Run time 7 min

NMV 50–5000

RIT 10–1000

ng/mL

NMV 50

RIT 10

ng/mL

NMV m/z 500.2→ 319.0,

RIT m/z 721.3 →267.8

[13]

  1. Bold illustrates important values