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 (2∶8)/ 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‑(3‑Trifluoromethylphenyl) piperazine and 1‑(3‑Chlorophenyl) 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 |
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Received on 03.06.2019 Accepted on 25.06.2019
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Asian J. Pharm. Res. 2019; 9(3):209-218.
DOI: 10.5958/2231-5691.2019.00035.2