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Chromatin Structure Regulates pre-mRNA Processing02:41

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In eukaryotic cells, nascent mRNA transcripts need to undergo many post-transcriptional modifications to reach the cell cytoplasm and translate into functional proteins. For a long time, transcription and pre-mRNA processing were considered two independent events that occur sequentially in the cell. However, it has now been well established that transcription and pre-mRNA processing are two simultaneous processes that are precisely regulated inside the cell.
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Metabolic reactions in the body produce nonvolatile acids, such as sulfuric acid, which generate an acid load of approximately 1 mEq of H+ per kilogram of body weight daily. Excreting H+ in the urine is essential to balance this acid load.
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Related Experiment Video

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Preparation of Chitosan-based Injectable Hydrogels and Its Application in 3D Cell Culture
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Onion-structure bionic hydrogel capsules based on chitosan for regulating doxorubicin release.

Wei Zhang1, Xin Jin1, Heng Li1

  • 1State Key Laboratory of Structure Analysis for Industrial Equipment, Department of Engineering Mechanics, Dalian University of Technology, Dalian 116024, China.

Carbohydrate Polymers
|February 9, 2019
PubMed
Summary

Novel multilayer hydrogel capsules, inspired by onions, effectively inhibit doxorubicin (DOX) burst release. These capsules offer controlled drug delivery and show pH sensitivity and biocompatibility for potential therapeutic applications.

Keywords:
Bionic multilayerBurst releaseDrug deliveryHydrogel capsulespH-sensitive

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Area of Science:

  • Biomaterials Science
  • Drug Delivery Systems
  • Nanotechnology

Background:

  • Burst release of drugs from hydrogel capsules leads to suboptimal therapeutic outcomes.
  • Developing strategies to control drug release is crucial for effective drug delivery systems.

Purpose of the Study:

  • To develop bionic multilayer hydrogel capsules for inhibiting the burst release of doxorubicin (DOX).
  • To investigate the drug distribution, release kinetics, pH sensitivity, and biocompatibility of the developed capsules.

Main Methods:

  • Fabrication of bionic multilayer hydrogel capsules using ionotropic crosslinking.
  • Characterization of DOX distribution and release profiles.
  • Assessment of pH sensitivity and biocompatibility with human epidermal keratinocyte (HaCaT) cells.

Main Results:

  • Multilayer hydrogel capsules homogenized DOX distribution and suppressed concentration gradients.
  • Significant inhibition of DOX burst release was achieved compared to monolayer capsules.
  • The capsules exhibited pH sensitivity and good biocompatibility with HaCaT cells.

Conclusions:

  • Bionic multilayer hydrogel capsules provide an effective strategy to control drug release.
  • This approach offers a promising platform for advanced drug delivery systems with enhanced therapeutic efficacy.