تصف هذه الدراسة طريقة كروماتوغرافيا سائلة عالية الأداء مؤشرة للثبات لمقايسة بنتوكسيفيلين في أشكاله الصيدليه. جرى فصل المادة الدوائية بنجاح عن نواتج التدرك، بعد تعريضها لشروط اجهاد، باستعمال عمود C18 و طور متحرك مكون من ماء و ميثانول (60: 40، حجم: حجم بتدفق 1 مل/د و طول موجة 272 نانومتر. كان زمن احتباس بنتوكسيفيلين نحو 14 دقيقة. جرى توثيق مصدوقية الطريقة فيما يتعلق بالخطية، الدقة، المضبوطية، و الانتقائية. أثبتت الخطية على مجال من 0.6 مكغ/مل الى 3.5 مكغ/مل و كان R2 0.994. كانت الطريقة مضبوطة (قيم استعادة 100.1%) و دقيقة (RSD > 2%). كان حد الكشف و حد الكم 0.2 مكغ/مل و 0.4 مكغ/مل على التوالي. طبقت الطريقة بنجاح لمقايسة بنتوكسيفيلين في المضغوطات مديدة التحرر المتوفرة في السوق السورية.
The present study describes a simple stability-indicating reversed-phase HPLC assay
for pentoxifylline in its pharmaceutical dosage forms. Separation of the drug and the
degradation products، under stress conditions was successfully achieved on a C18 column
utilizing water: MeOH (60:40 v/v)، pumped at a flow rate of 1 ml min-1 with UV detection
at 272 nm. The retention time of pentoxifylline was about 14 min. The method was
satisfactorily validated with respect to linearity، precision، accuracy and selectivity. The
response was linear in the range of 0.6-3.5 μg/ml with R2 0.994. The method was accurate
(recovery 100.1%) and precise (RSD < 2%). Detection and quantification limit were 0.2
μg/ml and 0.4 μg/ml respectively. The suggested method was successfully applied for the
analysis of pentoxifylline in extended release tablets available in Syrian market.
References used
Monteiro J. P.، Alves M. G.، Oliveira P. F.، Silva B. M.، Structure-Bioactivity Relationships of Methylxanthines: Trying to Make Sense of All the Promises and the Drawbacks. Molecules، Vol 21، 2016، ، 974-1006
McCarty M. F.، O'Keefe J. H.، DiNicolantonio J. J.، Pentoxifylline for vascular health: a brief review of the literature. Open Heart. Vol. 3، 2016، doi: 10.1136/openhrt-2015-000365
Bauza M.T.، Smith R. V.، Knutson D. E.، Witter F. R.، Gas chromatographic determination of pentoxifylline and its major metabolites in human breast milk. J. Chromatogr. Vol. 310، 1984، 61-69
The purpose of this work is to develop a sensitive, selective and validated
stability–indicating HPLC assay for the analysis of aspartame tablets.
Aspartame and its potential impurities or degradation products are
analyzed on C18 Column using a mo
A simple and rapid analytical method for routine quantification of Hyoscine
butyl bromide (scopolamine butyl bromide) in liquid oral formulations by highperformance
liquid chromatography was developed and validated. The oral
solution samples can be directly analyzed by reversed-phase HPLC on Intersil
ODS-3.
In this research two analytical methods were developed for the determination of Azelastin as raw material and in Nasal Spray formulation.
The first method was spectrophotometric while the other used the technic of HPLC The first method based on meas
Terfenadine reacts with mixed anhydriedes (Malonic and acetic anhydrides)
producing a yellow-coulored product with intense fluorescence. Based on this
fact, a spectrophotometric method was developed for the determination of
terfendaine in dosage f
New, accurate, sensitive and reliable kinetic spectrophotometric
method for the assay of fluvastatin sodium (FVS) in pure form and
capsules has been developed. The method involves the oxidative
coupling reaction of FVS with 3-methyl-2-benzothiazolinone hydrazone
hydrochloride monohydrate (MBTH) in the presence of Ce(IV) in an
acidic medium to form colored product with lambdamax at 615 nm.