Literature DB >> 16039810

Phase behavior of the microemulsions and the stability of the chloramphenicol in the microemulsion-based ocular drug delivery system.

Feng-Feng Lv1, Li-Qiang Zheng, Chen-Ho Tung.   

Abstract

Microemulsion systems composed of Span20/80+Tween20/80+n-butanol+H2O+isopropyl palmitate (IPP)/isopropyl myristate (IPM) were investigated as model systems of drug carriers for eye drops. Effects of chloramphenicol, normal saline, sodium hyaluronate and various oils on the phase behavior were studied. The phase transition was investigated by the electrical conductivity measurements. The electrical conductivity of the microemulsion was affected by the encapsulation of the drug into the system, and the addition of normal saline and sodium hyaluronate. The chloramphenicol is used to treat the diseases such as trachoma and keratitis. However, this drug in the common eye drops hydrolyzes easily. The main product of the hydrolysis is glycols. Here, the chloramphenicol was trapped into the oil-in-water (o/w) microemulsions and its stability was investigated by the high performance liquid chromatography (HPLC) assays in the accelerated experiments of 3 months. Its location in the microemulsion formulations was determined by means of 1H NMR spectroscopy. The results of HPLC revealed that the contents of the glycols in the microemulsion formulations were much lower than that in the commercial eye drops at the end of the accelerated experiments. It implied that the stability of the chloramphenicol in the microemulsion formulations was increased remarkably. The NMR experiments confirmed that the chloramphenicol molecules should be trapped into the hydrophilic shells of the microemulsion drops, which was composed of many oxyethylene groups. The nitro-groups of the chloramphenicol molecules were near the alpha2-CH2 of the surfactant molecules and the benzene rings of the chloramphenicol molecules were near the oxyethylene groups of the surfactant molecules. It was this reason that enabled the chloramphenicol molecules in the microemulsions to be screened from the bulk water and its stability to be increased remarkably.

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Year:  2005        PMID: 16039810     DOI: 10.1016/j.ijpharm.2005.06.006

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  9 in total

1.  Effect of lipolysis on drug release from self-microemulsifying drug delivery systems (SMEDDS) with different core/shell drug location.

Authors:  Jianbin Zhang; Yan Lv; Shan Zhao; Bing Wang; Mingqian Tan; Hongguo Xie; Guojun Lv; Xiaojun Ma
Journal:  AAPS PharmSciTech       Date:  2014-02-20       Impact factor: 3.246

2.  Incorporation of antitubercular drug isoniazid in pharmaceutically accepted microemulsion: effect on microstructure and physical parameters.

Authors:  S K Mehta; Gurpreet Kaur; K K Bhasin
Journal:  Pharm Res       Date:  2007-06-19       Impact factor: 4.200

3.  Stability, cutaneous delivery, and antioxidant potential of a lipoic acid and α-tocopherol codrug incorporated in microemulsions.

Authors:  Siji Thomas; Camila S Vieira; Martha A Hass; Luciana B Lopes
Journal:  J Pharm Sci       Date:  2014-06-24       Impact factor: 3.534

4.  Microemulsion system with improved loading of piroxicam: a study of microstructure.

Authors:  Muhammad Faizan Nazar; Asad Muhammad Khan; Syed Sakhawat Shah
Journal:  AAPS PharmSciTech       Date:  2009-10-30       Impact factor: 3.246

5.  Evaluation of Carbamazepine (CBZ) Supersaturatable Self-Microemulsifying (S-SMEDDS) Formulation In-vitro and In-vivo.

Authors:  Zhang Nan; Gao Lijun; Wang Tao; Quan Dongqin
Journal:  Iran J Pharm Res       Date:  2012       Impact factor: 1.696

6.  Optoacoustic/Fluorescent/Acoustic Imaging Probe Based on Air-Filled Bubbles Functionalized with Gold Nanorods and Fluorescein Isothiocyanate.

Authors:  Roman A Barmin; Polina G Rudakovskaya; Vasiliy S Chernyshev; Olga I Guslyakova; Pavel A Belcov; Ekaterina N Obukhova; Alexey V Gayer; Evgeny A Shirshin; Dmitry A Gorin
Journal:  ACS Omega       Date:  2021-01-25

7.  Microemulsion: new insights into the ocular drug delivery.

Authors:  Rahul Rama Hegde; Anurag Verma; Amitava Ghosh
Journal:  ISRN Pharm       Date:  2013-06-27

Review 8.  Ophthalmic Drug Delivery Systems for Antibiotherapy-A Review.

Authors:  Marion Dubald; Sandrine Bourgeois; Véronique Andrieu; Hatem Fessi
Journal:  Pharmaceutics       Date:  2018-01-13       Impact factor: 6.321

9.  Development of Triamcinolone Acetonide-Loaded Microemulsion as a Prospective Ophthalmic Delivery System for Treatment of Uveitis: In Vitro and In Vivo Evaluation.

Authors:  Alaa Mahran; Sayed Ismail; Ayat A Allam
Journal:  Pharmaceutics       Date:  2021-03-25       Impact factor: 6.321

  9 in total

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