1. Academic Validation
  2. ROS responsive hydrogel for inhibition of MUC5AC against allergic rhinitis: A new delivery strategy for Ipratropium Bromide

ROS responsive hydrogel for inhibition of MUC5AC against allergic rhinitis: A new delivery strategy for Ipratropium Bromide

  • Colloids Surf B Biointerfaces. 2024 Oct:242:114112. doi: 10.1016/j.colsurfb.2024.114112.
Qianqian Zhao 1 Min Gu 2 Mengnan Ni 1 Jinyu Li 1 Ting Wu 1 Senlin Zhu 1 Yupeng Zhou 1 Yawen Lu 1 Xiaolin Li 3 Huae Xu 4 Meiping Lu 5
Affiliations

Affiliations

  • 1 Department of Pharmaceutics, School of Pharmacy, Nanjing Medical University, Nanjing 211166, China.
  • 2 Department of Otorhinolaryngology & Clinical Allergy Center, The First Affiliated Hospital, Nanjing Medical University, Nanjing 210029, China.
  • 3 Department of Geriatric Gastroenterology, the First Affiliated Hospital of Nanjing Medical University, Nanjing 210009, China. Electronic address: lxl@njmu.edu.cn.
  • 4 Department of Pharmaceutics, School of Pharmacy, Nanjing Medical University, Nanjing 211166, China. Electronic address: xuhuae@njmu.edu.cn.
  • 5 Department of Otorhinolaryngology & Clinical Allergy Center, The First Affiliated Hospital, Nanjing Medical University, Nanjing 210029, China. Electronic address: lmp@njmu.edu.cn.
Abstract

Allergic rhinitis (AR) is a chronic inflammatory disease of the nasal mucosa mediated by immunoglobulin E (IgE) after exposure to allergens. The bothersome symptoms of AR, such as runny nose and nasal congestion, affect millions of people worldwide. Ipratropium Bromide (IB), commonly used in clinical practice for treating AR, requires frequent administration through nasal spray and may cause significant irritation to the nasal mucosa. The induction of ROS is closely related to the initiation and symptoms of AR, and ROS will continue to accumulate during the onset of AR. To address these challenges, we have designed a Drug Delivery system that can be administered in liquid form and rapidly crosslink into a ROS-responsive gel in the nasal cavity. This system enables sustained ROS responsive release of IB in a high-concentration ROS environment at AR lesions, thereby alleviating AR symptoms. The gel demonstrated prolonged release of IB for up to 24 hours in rats. In the treatment of AR rat models, it improved their symptoms, reduced the expression of various inflammatory factors, suppressed MUC5AC protein expression, and decreased mucus secretion through a ROS responsive IB release pattern. Overall, this system holds promise as a better option for AR treatment and may inspire the design of nanogel-based nasal Drug Delivery systems.

Keywords

Allergic rhinitis; Ipratropium Bromide; MUC5AC; ROS-responsive hydrogel.

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