Development of an RP-HPLC Method for Quantifying Diclofenac Diethylamine, Methyl Salicylate, and Capsaicin in Pharmaceutical Formulation and Skin Samples

被引:2
|
作者
AlNahwa, Lubna H. M. [1 ]
Ali, Hazim M. [1 ]
Hasanin, Tamer H. A. [1 ,2 ]
Shalaby, Khaled [3 ]
Alshammari, Mutairah S. [1 ]
Alsirhani, Alaa M. [1 ]
Mohamed, Sabrein H. [1 ,4 ]
机构
[1] Jouf Univ, Coll Sci, Dept Chem, POB 2014, Sakaka 72388, Aljouf, Saudi Arabia
[2] Minia Univ, Fac Sci, Dept Chem, Al Minya 61519, Egypt
[3] Jouf Univ, Coll Pharm, Dept Pharmaceut, POB 2014, Sakaka 72388, Aljouf, Saudi Arabia
[4] Cairo Univ, Fac Sci, Dept Chem, Giza 12613, Egypt
来源
MOLECULES | 2024年 / 29卷 / 12期
关键词
diclofenac diethylamine; methyl salicylate; capsaicin; Omni Hot Gel (R); RP-HPLC; VALIDATION; PARACETAMOL; SODIUM;
D O I
10.3390/molecules29122732
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
An RP-HPLC method with a UV detector was developed for the simultaneous quantification of diclofenac diethylamine, methyl salicylate, and capsaicin in a pharmaceutical formulation and rabbit skin samples. The separation was achieved using a Thermo Scientific ACCLAIM (TM) 120 C-18 column (Waltham, MA, USA, 4.6 mm x 150 mm, 5 mu m). The optimized elution phase consisted of deionized water adjusted to pH = 3 using phosphoric acid mixed with acetonitrile in a 35:65% (v/v) ratio with isocratic elution. The flow rate was set at 0.7 mL/min, and the detection was performed at 205 nm and 25 degrees C. The method exhibits good linearity for capsaicin (0.05-70.0 mu g/mL), methyl salicylate (0.05-100.0 mu g/mL), and diclofenac diethylamine (0.05-100.0 mu g/mL), with low LOD values (0.0249, 0.0271, and 0.0038 for capsaicin, methyl salicylate, and diclofenac diethylamine, respectively). The RSD% values were below 3.0%, indicating good precision. The overall greenness score of the method was 0.61, reflecting its environmentally friendly nature. The developed RP-HPLC method was successfully applied to analyze Omni Hot Gel (R) pharmaceutical formulation and rabbit skin permeation samples.
引用
收藏
页数:12
相关论文
共 50 条
  • [31] Stability-indicating RP-HPLC method development and validation for estimation of Mupirocin calcium in bulk and in pharmaceutical formulation
    Kalal, Durgeshwari J.
    Redasani, Vivekkumar K.
    FUTURE JOURNAL OF PHARMACEUTICAL SCIENCES, 2022, 8 (01)
  • [32] Stability-indicating RP-HPLC method development and validation for estimation of Mupirocin calcium in bulk and in pharmaceutical formulation
    Durgeshwari J. Kalal
    Vivekkumar K. Redasani
    Future Journal of Pharmaceutical Sciences, 8
  • [33] QbD Approach in RP-HPLC Method development for the Assay of Benzocaine and Diclofenac in dosage forms
    Manikandan, K.
    Lakshmi, K. S.
    Pai, Aswitha
    11TH NATIONAL CONFERENCE ON MATHEMATICAL TECHNIQUES AND APPLICATIONS, 2019, 2112
  • [34] RP-HPLC method development and validation for estimation of rivaroxaban in pharmaceutical dosage forms
    Celebier, Mustafa
    Recber, Tuba
    Kocak, Engin
    Altinoz, Sacide
    BRAZILIAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2013, 49 (02) : 359 - 366
  • [35] Development and validation of a RP-HPLC method for the simultaneous determination of paracetamol and diclofenac potassium on stainless steel surface of pharmaceutical manufacturing equipments
    Nag, Sindhur N.
    Gouthami, B.
    Madhuri, L.
    Krishnaveni, N.
    Meyyanathan, S.N.
    Suresh, B.
    Journal of Chemical and Pharmaceutical Research, 2012, 4 (03) : 1670 - 1675
  • [36] DEVELOPMENT AND VALIDATION OF STABILITY INDICATING RP-HPLC METHOD FOR DETERMINATION OF BROMELAIN, TRYPSIN, RUTOSIDE AND DICLOFENAC IN BULK AND PHARMACEUTICAL DOSAGE FORM
    Goday, Swapna
    Abdulrahaman, S. K.
    Prameelarani, A.
    INTERNATIONAL JOURNAL OF LIFE SCIENCE AND PHARMA RESEARCH, 2019, 9 (04): : P19 - P27
  • [37] Development and validation of a RP-HPLC method for the quantification of sparfloxacin in pharmaceutical dosage forms
    Sultan, Z.
    Zia-Ul-Huda, G.
    Hossain, A.
    Mazid, A.
    Rashid, A.
    ARS PHARMACEUTICA, 2012, 53 (01) : 11 - 16
  • [38] Development and Validation of rp-HPLC Method of Cabozantinib in Active Pharmaceutical Ingredient and Pharmaceutical Dosage form
    Chaudhary, Amruta A.
    Shelke, Ashwini, V
    Jadhav, Anil G.
    JOURNAL OF PHARMACEUTICAL RESEARCH INTERNATIONAL, 2021, 33 (11) : 81 - 90
  • [39] DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR THE ESTIMATION OF ANTIRETROVIRAL DRUGS AND THEIR PHARMACEUTICAL FORMULATIONS
    Joshi, Naresh Chandra
    Kumar, Pradeep
    Jat, Rakesh Kumar
    PHARMACOPHORE, 2016, 7 (03): : 152 - 165
  • [40] RP-HPLC Method Development and Validation of Tapentadol Hydrochloride in Bulk and Pharmaceutical Formulations
    Sangeetha, G.
    Manickam, M. Swamivel
    Kumar, P. Sanil
    JOURNAL OF PHARMACEUTICAL RESEARCH INTERNATIONAL, 2021, 33 (11) : 7 - 16