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Table 4 Stability-indicating method UHPLC-MS/MS

From: Ultra-high performance liquid chromatography-MS/MS (UHPLC-MS/MS) in practice: analysis of drugs and pharmaceutical formulations

Drug

Acid degradation

Base degradation

Photo-degradation

Oxidative degra.

Detection

Ref

Conditions

0.1 to 1 N

0.1 to 2 M

Light

H2O2 and KMnO4

Fluticasone Propionate

7 days

(50 °C) 24 h

Thioester, Carboxylic ester, alcohol, ketone, diol

[147]

Duloxetine

(50 °C) 24 h

7 days

Ether,1-naphthol

 

Amlodipine

24 h

24 h

1,4-dihydropyridine ring

 

Moxonidine

(0.5 M) HCl

80 min

2 M NaOH at 70 °C for 15 min

7 days at 80 °C

H2O2 5 h

Impurity-A and impurity-D

[148]

Rivaroxaban

(60 °C) 6–24 h

(60 °C) 1–6 h

2–5 h (254 nm)

Morpholinone moiety, oxazolidinone ring, chlorothiophene carbonyl.

[149]

Ciprofloxacin,Moxifloxacin, Norfloxacin, Ofloxacin

105–113 day

CP-1 - CP-6 and OP-1 - OP-6, NP-1 - NP-5 MP-1 and MP-10

[150]

Hexazinone

Degussa P25 and the nano-TiO2. 40 min complete degradation

Methylamine, triazinone, urea, carbon dioxide.

[151]

Ciprofloxacin, Difloxacin, Lomefloxacin, Norfloxacin, and Ofloxacin

KMnO4 in acidic pH (3–6)

N-1 and N-4 piperazine atoms and 3- monohydroxylated products 3-hydroxy-5-oxo derivatives

[152]

Ampicillin

(60 °C) 4 h

(60 °C) for 4 h

2-(acetamidomethyl)-5,5-dimethylthiazolidine-4-carboxylate 1, 1-dioxide

[153]