MICROENCAPSULATION OF BENZOYL PEROXIDE BY SUSPENSION POLYMERIZATION IN LIQUID-LIQUID SYSTEM METHOD

MICROENCAPSULATION OF BENZOYL PEROXIDE BY SUSPENSION POLYMERIZATION IN LIQUID-LIQUID SYSTEM METHOD


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نویسندگان: سیاوش دستمالچی , میترا جلوه گری , علی نخودچی , محمد رضا سیاهی شادباد

کلمات کلیدی: ANTI-ACNE, BENZOYL PEROXIDE, MICROSPONGES, METHYL METHACRYLATE, ETHYIEN GLYCOL DIMETHACRYLATE

نشریه: 27159 , 3 , 0 , 2005

اطلاعات کلی مقاله
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نویسنده ثبت کننده مقاله سیاوش دستمالچی
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه مرکز تحقیقات بیوتکنولوژی(زیست فناوری)
کد مقاله 59406
عنوان فارسی مقاله MICROENCAPSULATION OF BENZOYL PEROXIDE BY SUSPENSION POLYMERIZATION IN LIQUID-LIQUID SYSTEM METHOD
عنوان لاتین مقاله MICROENCAPSULATION OF BENZOYL PEROXIDE BY SUSPENSION POLYMERIZATION IN LIQUID-LIQUID SYSTEM METHOD
ناشر 4
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ بلی
عنوان نشریه (خارج از لیست فوق)
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح سه – Scopus
آدرس لینک مقاله/ همایش در شبکه اینترنت http://en.journals.sid.ir/ViewPaper.aspx?ID=79238

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Objective: Benzoyl peroxide (BPO) is commonly used in topical formulations for the treatment of acne. Skin irritation is a common side effect, and it has been shown that controlled release of BPO from a delivery system to the skin could increase patient compliance and reduce the side effect while reducing percutaneous absorptioo. Method: In this study, MMA/EGDM copolymer was prepared by monomers methyl methacrylate and ethylene glycol dimethaaylate. After impregnating copolymer MMA/EGDM, microsponges were evaluated in respect to morphology, particle size, volume, pore size and molecular weight characteristics. Releases of drug from microsponges were investigated using Cell-Franz with dialysis membrane and drug release was determined by HPLC. Results: The results showed that the cumulative amount of release increased with an increase in the concentration of the active ingredient in the formula. The amount of drug released at the first hour was higher compared to its released amount at 2ndh. This could be due to the presence of non encapsulated BPO in these formulations. When the free BPO was released, the flux remained constant for the next 7 hrs. CONCLUSION: This flux represents the release of entrapped drug from microsponges. Released BPO in different dosage forms was respectively lotion < gel < cream. The topical microsponge delivery system can clearly maximize the amount of time that an active ingredient presents on the skin surface within the epidermis, therefore, into the body.

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نویسنده نفر چندم مقاله
سیاوش دستمالچیچهارم
میترا جلوه گریاول
علی نخودچیدوم
محمد رضا سیاهی شادبادسوم

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55.png1395/08/2952362دانلود