Recent Analytical Methods of Anti-Helmintic Agents
 
Sonali Mahaparale*, Diksha Banju
Department of Pharmaceutical Chemistry, Dr. D. Y. Patil College of Pharmacy, Akurdi, Pune, Maharashtra, India.

*Corresponding Author E-mail: mahaparalesonali40@gmail.com

 

ABSTRACT:

Infections with helminths, or parasitic worms, affect more than two billion people worldwide. Anthelmintic are drugs that either kill vermicide or expel vermifuge infesting helminths. Helminthiasis is prevalent globally. classification of anthelmintic based on chemical stricture piperazines: diethylcarbamazine citrate piperazine citrate. benzimidazoles: albendazoles, mebendazoles, thiabendazoles. etc. albendazole a broad spectrum oral anthelmintic agent it is the drug of choice for treatment of hydatid disease and cysticercosis. Diethylcarbamazine has a highly selective effect on microfilariae. IUPAC name for Niclosamide is 5-chloro-N-(2chloro-4-nitrophenyl)-2-hydroxybenzamide. Current review highlights that research work done under the category of anthelmintic drugs

 

KEYWORDS: Anthelmintic, HPLC, UV, Albendazole, helminthiasis.

 

 


INTRODUCTION:

Antihelmintics are drugs that are used to treat infections with parasitic worms. This includes each flat worms, e.g., flukes and tapeworms and round worms, i.e., nematodes. They are of big importance for human medicine and for medicine. The World Health Organization estimates that stunning or killing them and without causing significant damage to the host [2]. Helminths can be a staggering 2 billion people harbour parasitic worm infections [1]. Anthelmintic drugs are substances that expel or destroys worms and other internal parasites from the body by either divided into 3 groups: cestodes or tapeworms: nematodes or roundworms: and trematodes or flukes. The helminths take issue from different infectious organisms therein they need a fancy bodily structure.

 

 

They are multicellular and have partial or complete organ system (e.g., muscular, nervous, digestive, and reproductive). Several of the drugs used to treat worm infections effect the nervous system of the parasite and result in muscle paralysis [3]. Helminthiasis is more common in developing countries with poorer personal and environment hygiene. In the human body GIT is the abode of many helminths, nut some also live in tissues, or their larvae migrate into tissues. Helminthiasis is never fatal, however could be a major explanation for unwell health [4].

 

History:

Albendazole is orally administered anthelmintic drug. Chemically it is methyl 5(propylthio)-2benzimidazolecarbamate. Molecular formula of Albendazole is C12H15N3O2S and molecular weight is 265.34. Albendazole is available in the market in the form of tablets and oral suspensions [5]. Albendazole is a benzimidazole class of drug being used in the treatment for parasitic infections. It is a broad spectrum anthelmintic effective against roundworms, tapeworms, and flukes of domestic animals and humans [6]. Mebendazole (fig;2) was methyl (5-benzoyl-1H-benzimidazol-2-yl) carbamate, Mebendazole is thought to work by selectively inhibiting the synthesis of microtubules in parasitic worms, and by destroying extant cytoplasmic microtubes in their intestinal cells, thereby blocking the uptake of glucose and other nutrients, resulting in the gradual immobilization and eventual death of the helminthes [7]. Thiabendazole is broad spectrum antihelmintic agent used predominantly in treatment of intestinal pinworm and strongyloides infection, which recently has been replaced by better tolerated agents. Thiabendazole therapy has been shown to cause clinically apparent cholestatic liver injury which is rare, but can be severe [8]. Its chemical structure 2-(1,3-thiazol-4-yl)-1H-1,3-benzodiazole. Thiabendazole is a fungicide and parasiticide. Thiabendazole is also a chelating poisoning or antimony poisoning [9]. Diethylcarbamazine citrate (DEC) chemically, N, N-diethyl-4methylpiperazine-1-carboxamide dihydrogen citrate. It is a anthelminthic anthelmintic agent indicated for the treatment of individual patients with body fluid disease, tropical pulmonic symptom and loiasis. It acts by inhibiting arachidonic acid metabolism [10]. Piperazine is a cyclic organic compound possessing two nitrogen atoms in opposite positions within a 6-member heterocyclic ring that serves as a backbone for piperazine derivatives and acts as a gamma-amino-butyric acid (GABA) receptor agonist in nematodes, with potential anti-helminthic activity [11]. Niclosamide is within the antihelminthic family particularly effective against cestodes that infect humans. It is also used as a pesticide, Niclosamide is used specifically to treat tapeworms and is not effective against other worms such as pinworms or roundworms. IUPAC name for Niclosamide is 5-chloro-N-(2chloro-4-nitrophenyl)-2-hydroxybenzamide [12]. Pyrantel pamoate is chemically named as 4[(3-Carboxy-2-hydroxynaphthalen-1-yl)methyl]-3hydroxynaphthalene -2-carboxylic acid; 1-methyl-2[(E)-2-thiophen-2-ylethenyl]-5, 6-dihydro-4Hpyrimidine. It is used as a deworming agent in the treatment of hookworms (all species) and roundworms (Ascaris lumbricoides, aka ascarids in humans) in domesticated animals such as horses, cattle, sheep, pigs, cats, dogs, and many other species [13]. Praziquantel is a pyrazinoisoquinoline derivative [2-(cyclohexyl-carbonyl)-1,2,3,6,7,11 bhexahydro-4H-pyrazino[2,1-a]isoquinoline-4-one],

which is the treatment of choice for most human trematode and cestode infections, and is widely used in schistosomiasis, as well as other fluke infections pathogenic to human[14]. Levamisole is a white or almost white powder, slightly soluble in water, freely soluble in alcohol and in methanol (The British Pharmacopoeia, 2011). Levamisole is the active levoisomer of tetramisole. It is used as an anthelmintic and as an adjuvant in malignant disease [15].

 


HPLC

Drug

Column

Mobile phase (v/v)/ Detection (nm)

Flow rate (mL/min)

Ref

Albendazole

L11, 150 x 4.6mm, 5µm

acetonitrile, methanol and water in the ratio of (50:40:10)/ 254

 

16

Albendazole And CLOSANTEL

Hypersil BDS C18 (150 x 4.6 mm, 5μ)

acetonitrile: D.W.: methanol (60:30:10)/ 254

1.8

17

Albendazole and Ivermectin

NUCLEODUR C18 (250 x 4.6mm, 5 μ)

ACN: methanol: water (60:30:10)/ 245

1.8

18

Albendazole suspension of Rombendazo

Kromasil C18 (150 mm x 4.6 mm i.e.; 5 μm)

Methanol: Distilled water (65:35)

1.2

19

Albendazole and praziquantel

Inertsil ODS, C-18,250×4.6mm ID, 5µm

Phosphate Buffer pH 4.0: Acetonitrile: Methanol (20:70:10)/ 238

1.0

20

Albendazole and Ivermectin

INERTSIL C18 BDS column (250 x 4.6 mm, 5 µ)

Acetonitrile: methanol and water (40:60)/ 280

1.0

21

Albendazole and Ivermectin

SupelcosilTM (150 x 4.6 mm i.d.,5 µ)

Acetonitrile: Methanol: Buffer (pH 7.0) (51:25:24)

 

22

Albendazol and Triclabendazol

Lichrosorb RP-18 (5 μm) (250 × 4 mm)

Acetonitrile: ammonium acetate buffer solution of pH 6.6 (70:30)/ 298

 

23

MEBENDAZOLE

Aglient C18 250 x 4.6 mm, 5 μ

ACN: water pH 3.0 with OPA (90:10)/ 234

1.0

24

Mebendazole, Methylparaben and Propylparaben

(Inertsil ODS-3V) C18 Column (250mm × 4.6mm, 5μm particle size)

Methanol: 0.05M monobasic potassium phosphate: Acetonitrile (48:32:20)/247

1.5

25

Mebendazole and Levamisole

C18 column, zodiac 5µ (4.6×250mm)

Methanol: Acetonitrile (30:20:50)/ 235

1.0

26

Thiabendazole

ACE 5 C18 (4.6 x 50 mm, 5 μm particle size)

25% acetonitrile and 75% 10 mM 1-octanesulfonic acid sodium salt aqueous/ 300

1.5

27

Thiabendazole and mebendazole

C18 column

KH 2PO4 0.05 mol L-1 and methanol (40:60)/ 312

-

28

CHLORPHENIRAMINE MALEATE + DIETHYL

CARBAMAZINE CITRATE

Kromasil C18 (250 x 4.6mm, 5μm particle

size

(80:20) Acetonitrile: Potassium di hydrogen phosphate solution (0.01M, pH 3.0

adjusting with Ortho phosphoric acid

1.0

29

DIETHYL

CARBAMAZINE

Phenomenex C8 column (15 cm×4.6 mm) of 5 μm particle

Size

Acetonitrilel: Phosphate buffer (20 mM KH2PO4, adjusted to pH 3.2 with 10% ortho-phosphoric acid)

in the ratio of (1:9)

1.5

30

DIETHYL

CARBAMAZINE+ Levocetirizine

Princeton Sphere-100 C18 (250×4.6 mm. 5 μ)

20mM potassium dihydrogen orthophosphate buffer (pH: 3.2): acetonitrile (50:50 v/v)

1.0

31

DIETHYLCARBAMAZINE CITRATE, GUAIPHENESIN AND CHLORPHENIRAMINE MALEATE

luna phenyl-hexyl column (250 mmx4.6 mm, dp=5 μm)

0.1% triethylamine as buffer along with orthophosphoric acid adjusted to PH 2.5: acetonitrile (50:50v/v)

1.0

32

DIETHYLCARBAMAZINE AND LEVO-CETIRIZINE

Hypersil-BDS C18 (250×4.6 mm. 5 μ) column

potassium dihydrogen orthophosphate buffer (pH: 5): acetonitrile (20:80 v/v)

and the pH was adjusted with orthophosphoric acid

1.0

33

Diethylcarbamazine Citrate and Cetirizine Hydrochloride

 

C18 phenomenexluna (250 × 4.6, 5μm)

0.05 M Phosphate buffer and Acetonitirile (pH 3) in the ratio of 60: 40 v/v.

1.0

34

Diethylcarbamazine

Citrate and Chlorpheniramine Maleate

hypersil ODS-C18 (5μ,

250 mm x 4.6 mm

methanol: buffer (55:45v/v)

(The combination of DEC and CPM used)

1.0

35

Phenobarbital and Acefylline Piperazine

Thermo Hypersil C18 gold column

 

Acetonitrile - 0.1% orthophosphoric acid (30:70, v/v)

1.5

36

Piperazine

Chiralpak IC (Diacel) of dimensions 250 X4.6 mm, 5μm

Acetonitrile, Methanol and diethyl amine in the ratio of 90:10:0.1(v/v/v).

1.0

37

Piperazine

Alltech AlltimaCyano (2504.6 mm) column

Naproxen piperazine 27.22 (1: 1)

Naproxen hemipiperazine 15.76 (2: 1)

Phenylbutazone hemipiperazine 12.26 (2: 1)

Phenylbutazone piperazine 21.83 (1: 1)

0.5

38

Piperazine

C18

column (Waters Xbridge; 4.6 mm × 250 mm, particle size, 5 μm; Waters, Milford, MA, USA)

water and ACN (30:70, v/v).

1.0

39

Niclosamide

Zorbax C 18 (250×4.6, 5µm)

Potassium phosphate buffer: Acetonitrile (60:40)/ 290

 

40

Niclosamide

C-18 column (250nm x 4.66nm, 5 µm)

Methanol: 1mM ammonium phosphate buffer (85:15)/ 332

 

1.2

41

Niclosamide

Zorbax C18 (250×4.6, 5µm)

Potassium dihydrogen phosphate buffer: Acetonitrile (60:40)/ 290

1.0

42

Niclosamide and Fenbendazole

L1 C18 100 A° column (250 x 4.6 mm, 5 μ)

potassium dihydrogen phosphate and acetonitrile (70:30)/ 290

1.0

43

Niclosamide and Levamisole Hydrochloride

Luna C18

Acetonitrile: buffer solutions (28)/ 240

 

44

Pyrantel Pamoate, Praziquantel, Fenbendazole, Oxfendazole and

Butylhydroxyanisole

Phenomenex Luna 3

mm phenyl–hexyl column (150×3.0 mm)

0.5% triethylamine at

pH 9.0 and acetonitrile 55: 45 (v/v)/ 220

1.0 ml/min-1

45

Praziquantel and Pyrantel Pamoate

Kromasil 60-5SIL. (250 mm x 4,6 mm i.d.; 5 5m particle size) Phenomenex

acetonitrile/distilled water (60/ 40 v/ v)/ 210

1.0 ml/min

46

Pyrantel Pamoate and Praziquantel

Luna C18 column (250 mm × 4.6 mm, 5 μm)

 

Water: Acetonitrile (20: 80)/ 220

1.0 ml/min

47

Oxantel Pamoate, Pyrantel Pamoat and Praziquantel

Reversed–Phase Column (4.6 X 150 Mm,

5 Μm) C18

ACN: MeOH:20 mM

phosphate buffer (0.2 % TEA, pH 4.5) (50:10:40, v/v/v)/ 210

1.0 ml/min

48

Oxantel and Pyrantel Pamoate

150-mm χ 4.6-mm octyl Spherisorb® column (reversedphase,

particle size 5 μm)

(42% v/v) and

water (58% v/v) containing 0.1 Μ n-butylamine, pH adjusted/ 313

to 3.0 with perchloric acid

1.0 ml/min

49

Pyrantel Pamoate and Febantel

 

Hypersil BDS C18 (150 × 4.6 mm, 5 μ) column

acetonitrile: phosphate buffer in the ratio 85:15% v/v and 55:45% v/v with apparent pH adjusted and maintained to 3.5 using 0.01M orthophosphoric acid/ 286

1.0 ml/min

50

Pyrantel Pamoate and Albendazole

BDS C-18 column (4.6 x 250mm, 5μ particle size)

0.1% Potassium dihyrogen Ortho phosphate (adjusted to pH 4.8 with triethylamine solution), Acetonitrile, methanol (40:40:20v/v)/ 311

1.0 ml/min

51

Ofalbendazole and Praziquantel

Enable C18column (250 mm × 4.6 mm, 5 m

 

Acetonitrile - 0.1% orthophosphoric acid (30:70, v/v)/ 225

1.0 ml/min

52

Praziquantel

(Caltrex

AI) Calixarene column

ACN and 25 mM ammonium acetate (NH4Ac) in the ratio

of 40:60/ 210

1.0 ml/min

53

Pyrantel Pamoate, Praziquantel, Fenbendazole, Oxfendazole and

Butylhydroxyanisole

Phenomenex Luna 3

mm phenyl–hexyl column (150×3.0 mm)

0.5% triethylamine at

pH 9.0 and acetonitrile 55: 45 (v/v)/ 220

1.0 ml/min

54

Pyrantel Pamoate and Praziquantel

Luna C18 column (250 mm × 4.6 mm, 5 μm)

Water: Acetonitrile (20: 80)/ 220

1.0 ml/min

55

Praziquantel

C18 column Enable (250mm × 4.6 mm, 5μm)

acetonitrile and distilled water (60:40, v/v)/ 225

1.0 ml/min

56

Praziquantel

Luna C18 column (250mm × 4.6 mm,

5m particle size)

acetonitrile and distilled water (70:30, v/v)/ 217

1.0 ml/min

57

Praziquantel

Enable, C18 column

(250×4.6 mm, 5 μm particle size)

acetonitrile: water in a ratio of (60:40 v/v)/ 225

1.0 ml/min

58

Oxantel Pamoate, Pyrantel Pamoat and Praziquantel

reversed–phase column (4.6 x 150 mm,

5 μm) C18

ACN: MeOH:20 mM

phosphate buffer (0.2 % TEA, pH 4.5) (50:10:40, v/v/v)/ 210

1.5 ml/min

59

Levamisole

(250 X 4.6 mm I.D.) packed with

TSK-GEL LS 410 ODS SIL (Cl8 chemically bonded silica gel, particle size

5 pm)

methanol-0.05 M ammonium carbonate solution

(65:35, v/v)/ 232

1.0 ml/min

60

Linezolid and

Levamisole Hydrochloride

Genesis® C18 column (250 mm × 4.6 mm id,

4 μm, BDS 120 Å)

Ammonium acetate and

acetonitrile in the ratio 65:35 (%v/v)/ 236

0.9 ml/min

61

Oxyclozanide and Levamisole

X Bridge, size 150×4.6 mm, C18, particle size

3.5μm.

acetonitrile: methanol: 0.05M potassium

dihydrogen phosphate in ratio (60:20:20)/ 220

1.0 ml/min

62

LEVAMISOLE

Welchrom C18 isocratic column, (250 mm × 4.6 mm

Methanol: Acetonitrile: Water 50:30:20 v/v, with apparent pH of 4.6/ 225

1.0 ml/min

63

Levamisole and Albendazole

 

Inertsil ODS C18 (4.6 x 150 mm, 5 𝜇m)

pH 3.5 and acetonitrile (70:30 v/v)/ 224

1.0 ml/min

64

Oxyclozanide and Levamisole Hcl

Thermo

C18 (250 x 4.6 mm)

Acetonitrile: Methanol: Water in a ratio of 50:30:20 v/v/ 220

1.0 ml/min

65

Levamisole

YMC C18 column

(250 x 4.6mm, 5 μ particle size)

Acetonitrile and water in the ratio of 80:20%V/V/ 217

0.7ml / min

66

Levamisole and Mebendazole

 

C18 column, zodiac 5μ (4.6×250mm).

pH 5.2: Methanol: Acetonitrile (30:20:50 v/v/v)/ 235

1.0 ml/min

67

Levamisole Hydrochloride and Anhydrous

Niclosamide

Luna C-18 column

acetonitrile–buffer

solutions (2:8, v/v)/ 240

0.7ml / min

68

 

TITRIMETRIC+SPECTROPHOTOMETRIC

Drug

Method

Reagent

λ (nm)

Linearity (µg/mL)

Ref

Albendazole

UV

ethanolic HCl

308

4-10

69

ALBENDAZOLE

UV

0.1N HCL

229

4-20

70

Albendazole

UV

Methanolic glacial acetic acid

235

2.5-20

71

Albendazole

UV

Double distilled water

295

5-25

72

ALBENDAZOLE

UV

HcL

482

10-110

73

Albendazole and Ivermectin

UV

1N HcL

248.8

314.4

5-40

74

Mebendazole

UV

 

234

1-10

75

MEBENDAZOLE AND LEVAMISOLE HYDROCHLORIDE

UV

1% H2SO4 in methanol

307

2-6

76

Levamisole HcL

Uv

methanol

213

2-14

77

Levamisole HcL

Uv

Distilled water

215

2-10

78

Levamisole HcL and Albendazole

Uv

Ammonium dihydrogen phosphate: methanol

213

295

2-10

79

Diethylcarbamazine Citrate

Titrimetric &

UV

Permanganate

545 nm

2.5-30 μg mL-1 + 1-10 mg

80

Diethyl

Carbamazine

Titrimetric &

UV

N-bromosuccinimide

490 nm

15-120 μg mL-1+ 3-18 mg

81

Diethylcarbamazine

citrate

Titrimetric &

UV

Iodate and Iodide

 

570 nm

2.5-50 mg and 2.5-30 μg mL-1

82

Chlorpheniramine Maleate and

Diethylcarbamazine Citrate

UV

0.01N sodium hydroxide

216nm and 261nm

10-50 μg mL-1

83

Piperazine, Piperazine Salts and

Diethylcarbamazine Citrate

UV

Chloranilic Acid

345 nm

1-10

84

Diethylcarbamazine Citrate

UV

Folin-Ciocalteu Phenol

760 nm

10-100

85

PIPERAZINE

UV

Pphenothiazine and N-bromosuccinimide

595 nm

0.5-5 μg/ml and 0.5-3 μg/ml

86

Piperazine

UV

Chloronil

545 nm

0.1-0.8 mg and 2 ml

87

Piperazine, Piperazine Salts and

Diethylcarbamazine Citrate

UV

Chloranilic Acid

345 nm

1-10 μg/ml

88

Niclosamide

UV

Methanol

243

25-150

89

Niclosamide

UV

1 M hydrochloric acid, 0.75 ml 1% sodium nitrite solutions, 0.5 ml 3% sulphamic acid solution, 2 ml 0.1 % 2,6 dihydroxybenzoic acid reagent solution, 0.6 ml of 1M NaOH are added.

456

5-300

90

Niclosamide and fenbendazole

UV

0.1 N Methanolic HCl

317 and 226

 

3-9

91

Pyrantel Pamoate Using Iron (III) Chloride

UV

ferricyanide (method A), 1, 10-phenanthroline (method B) and 2,2’-bipyridyl (method C).

750, 520 and 530 nm,

3.0-35, 1.0-30 and 2.0-35 μg mL-1

92

Pyrantel in Pyrantel

Pamoate

UV

Ammonium hydroxide, 1,4-dioxane, perchloric acid,

Hhydrochloric acid, and Chloroform

311 nm

-

93

PYRANTEL PAMOATE

UV

PYL solution

380, 420 and 430 nm

0.1- 2.5 ml(Method-A)

0.1- 3.25 (Method-B)

0.1- 2.5 ml(Method-C)

94

Pyrantel Pamoate

UV

Phenol red and Thymol blue

430 and420 nm

0.02-0.5 and 0.05-0.8 μg ml–1

95

Albendazole and

Praziquantel

UV

Methanol

210 nm

10-130% (0.665-9.972 mg L-1).

96

Praziquantel

UV

Methyl alcohol

287.2nm-

236.6 nm

10:1

97

Oxyclozanide and Levamisole

UV

methanol, ammonium

hydroxide and potassium dihydrogen phosphat

220 nm

5-40 μg/ml

98

Levamisole

Hydrochloride

UV

Distilled Water

215nm

2-10 μg/ml

99

 

COLORIMETRIC

Drug

Detection (nm)

Linearity (μg/mL)

Buffered

Ref

PIPERAZINE

516 nm

4-20 ug/ml

pH 5.4

100

Antibilharzial Drug Praziquantel

550, 425, 460, 844 and 393nm

2.0-48 mgml-1

Ethanol

101

 

SPECTROFLUORIMETRY

Drug

Detection (nm)

Buffers

Linearity (μg/mL)

Reagent

Ref

Praziquantel

263 nm

acetate buffers (pH 3.7-4.7) and phosphate buffers (pH 5.8-

7.8)

1-20 μg/mL

Water

102

 

GC

Drug

Column

Carrier gas

Air flow

Injection mode

Diluent

Linearity

(mg/mL)

Ref

Piperazine, 1-Methyl Piperazine and 1-Ethyl Piperazine

DB-17equivalent toUSP

Phase G3[(50%-Phenyl)-methylpolysiloxane] (30

m×0.53mm, 1μm) capillarycolumn

Helium

40mL/min andHydrogen flow of

400mL/min.

Split

modewith a split ratio of 1:5.

Methanol

25 -1 to 150

103

1(3Trifluoromethylphenyl)

piperazine and 1(3Chlorophenyl) piperazine

D B 5 M S

(30 m × 0.25 mm × 0.25 µm)

Nitrogen

15 mL/min

Split flow, split ratio is 15:1

Methanol

0.1- 100

104

Piperazine

30 m x 0.3 mm i.d fused silica column coated with

a 3.0 Ltrn film of 5% cross linked Ph-Me silicone

Nitrogen

1 ml min

-

Methanol

0.4-10 ppm

105

Levamisole

Agilent DB-5MS UI column (30 m ×

0.25 mm, 0.25-μm film thickness

Helium

1 mL/min.

Splitless

injection for 1 min

 

6 - 8300

106

 

HPTLC

Durg

Method

Mobile Phase

λ (nm)

Ref

Albendazole

TLC

dichloromethane: methanol (90:10)

232

107

Albendazole

TLC

dichloromethane: methanol (90:10)

232

108

Albendazole and albendazole sulfoxide

HPTLC

Toluene: acetonitrile: glacial acetic acid (7.0:2.9:0.1)

225

109

Niclosamide

HPTLC

Toluene: ethyl acetate (7:3)

332

110

Oxyclozanide And Levamisole Hydrochloride

HPTLC

Toluene: acetone: ammonia (5:5:0.04 v/v/v)

225 nm.

111

Oxyclozanide And Levamisole HCl

HPTLC

Ethyl acetate: Ammonia: TEA: Methanol (6:0.5:0.2:0.5 v/v)

220 nm

112

Levamisole

TLC

methanol: water: 0.1% acetic acid (7:2.5:0.5, v/v/v)

213 nm

113

 

LCMS

Drug

Column

Mobile phase (v/v) / Detection

wavelength (nm)

Flow rate (mL/min)

λ (nm)

Ref

Diethyl

Carbamazine Citrate and Chlorpheniramine Maleate

Sunfre C18, 5 (im (250 mmx 4.6 mm i.d.)

water: methanol: 10% triethyl amine (10:90:0.1, v/v; pH 5.5)

1.0 ml/min

225 nm.

114

diethylcarbamazine, albendazole

and albendazole metabolites

UPLC®BEH C18 column (100 x 2.1 mm, 1.7 μm) with

0.05 % formic acid

in methanol and 0.05 % formic acid

0.2 ml/min

-

115

Ivermectin, Febantel, Praziquantel, Pyrantel pamoate

C8 column (50 x 2.1 mm i.d) coupled with a C8 (10 x 2.1 mm i.d) guard column

Water/Acetonitrile (15:85 v/v) containing 0.1% formic acid and 3 mmol/L ammonium formate.

200 μL/min.-1

-

116

 

MASS

Drug

Column

Mobile phase (v/v) / Detection

wavelength (nm)

Flow rate (mL/min)

Linearity Range

Ref

Levamisole

Poroshell 120

EC C18, 50x3 mm, 2.7 μm particle size

0.1 % formic acid; 0.1 % formic acid

in acetonitrile

0.3 mL min-1

5, 25, 50, 100 and

150 μg L-1

117

Levamisole

GAgilent DB-5MS UI column (30 m × 0.25 mm

1 M sodium hydroxide

and 95:5 hexane/isoamyl alcohol extraction

-

6–223 ng/mL

118

 


REFERENCE:

1.     Http://Www.Wormbook.Org/Chapters/Www_Anthelminticdrugs/Anthelminticdrugs.Html.

2.     Https://Www.Sciencedirect.Com/Topics/Chemistry/Anthelmintic-Ag.Ent.

3.     Https://Www.Britannica.Com/Science/Anthelmintic.

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Received on 03.06.2019        Accepted on 25.06.2019

© Asian Pharma Press All Right Reserved

Asian J. Pharm. Res. 2019; 9(3):209-218.

DOI: 10.5958/2231-5691.2019.00035.2