Published July 27, 2018 | Version v1
Journal article

Effect of taste masking technology on fast dissolving oral film: dissolution rate and bioavailability

  • 1. State Key Laboratory of Natural Medicines, China Pharmaceutical University, No. 24 Tongjia Xiang, Nanjing, 210009 (China)
  • 2. Key Laboratory of Sensing Technology and Biomedical Instrument of Guangdong Province, School of Engineering, Sun Yat-sen University, Guangzhou, 510006 (China)
  • 3. Nanjing iPharma Technology Co. Ltd, No. 68 Zhushan Road, Nanjing, 211100 (China)
  • 4. University of Waterloo, 200 University Ave W, Waterloo, ON N2L 3G1 (Canada)
  • 5. Department of Orthopedics, Xinqiao Hospital, Third Military Medical University, Chongqing,400037 (China)
  • 6. Key Laboratory of Mountain Ecological Restoration and Bioresource Utilization, Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu, 610041 (China)

Description

Fast dissolving oral film is a stamp-style, drug-loaded polymer film with rapid disintegration and dissolution. This new kind of drug delivery system requires effective taste masking technology. Suspension intermediate and liposome intermediate were prepared, respectively, for the formulation of two kinds of fast dissolving oral films with the aim of studying the effect of taste masking technology on the bioavailability of oral films. Loratadine was selected as the model drug. The surface pH of the films was close to neutral, avoiding oral mucosal irritation or side effects. The thickness of a 2 cm × 2 cm suspension oral film containing 10 mg of loratadine was 100 μm. Electron microscope analysis showed that liposomes were spherical before and after re-dissolution, and drugs with obvious bitterness could be masked by the encapsulation of liposomes. Dissolution of the two films was superior to that of the commercial tablets. Rat pharmacokinetic experiments showed that the oral bioavailability of the suspension film was significantly higher than that of the commercial tablets, and the relative bioavailability of the suspension film was 175%. Liposomal film produced a certain amount of improvement in bioavailability, but lower than that of the suspension film. (paper)

Availability note (English)

Available from http://dx.doi.org/10.1088/1361-6528/aac010

Additional details

Identifiers

Publishing Information

Journal Title
Nanotechnology (Print)
Journal Volume
29
Journal Issue
30
Journal Page Range
[12 p.]
ISSN
0957-4484

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
51058123
Subject category
S77: NANOSCIENCE AND NANOTECHNOLOGY;
Descriptors DEI
BIOLOGICAL AVAILABILITY; DISSOLUTION; DRUG DELIVERY; DRUGS; ELECTRON MICROSCOPES; ENCAPSULATION; FILMS; LIPOSOMES; PH VALUE; POLYMERS; RATS; RESPIRATORS; SURFACES; SUSPENSIONS; THICKNESS
Descriptors DEC
ANIMALS; DIMENSIONS; DISPERSIONS; MAMMALS; MICROSCOPES; RODENTS; VERTEBRATES