Next Article in Journal
Enhanced Cellular Uptake of H-Chain Human Ferritin Containing Gold Nanoparticles
Next Article in Special Issue
Internalization and Transport of PEGylated Lipid-Based Mixed Micelles across Caco-2 Cells Mediated by Scavenger Receptor B1
Previous Article in Journal
Encapsulation of Asparaginase as a Promising Strategy to Improve In Vivo Drug Performance
Previous Article in Special Issue
Retinoic Acid-Containing Liposomes for the Induction of Antigen-Specific Regulatory T Cells as a Treatment for Autoimmune Diseases
 
 
Article
Peer-Review Record

Aliphatic Quaternary Ammonium Functionalized Nanogels for Gene Delivery

Pharmaceutics 2021, 13(11), 1964; https://doi.org/10.3390/pharmaceutics13111964
by Huaiying Zhang, Damla Keskin, Willy H. de Haan-Visser, Guangyue Zu, Patrick van Rijn * and Inge S. Zuhorn *
Reviewer 1: Anonymous
Reviewer 2: Anonymous
Pharmaceutics 2021, 13(11), 1964; https://doi.org/10.3390/pharmaceutics13111964
Submission received: 21 October 2021 / Revised: 12 November 2021 / Accepted: 16 November 2021 / Published: 19 November 2021
(This article belongs to the Collection Drug Delivery in The Netherlands)

Round 1

Reviewer 1 Report

The paper liphatic quaternary ammonium functionalized nanogels for gene delivery, prepared by Huaiying Zhang et al., presents novel and interesting results that deserve to be published after some minor improvements:

  1. font size of figure 1 must be increased.
  2. Same issue in figure 4-B
  3. Figure 5 -  there are figures where the scale bar is missing.
  4. Figure 4 - same issue.
  5. Figure 6 - same issue

 

Author Response

please see the attachment

Author Response File: Author Response.docx

Reviewer 2 Report

The manuscript entitled “Aliphatic quaternary ammonium functionalized nanogels for gene delivery”, by Zhang et al have prepared and characterized poly(N-iso-propylacrylamide) nanogels with varying cationic functionalities and tested them in vitro in HEK293T cell culture for cytotoxicity, cellular uptake, transfection, and mechanism of cellular escape. The research is well designed and executed. The data supports the conclusions obtained. Although the work is very preliminary, it is intriguing. There are a few minor comments for the authors as noted below.

Comments to authors:

  1. Authors should perform additional experiments with well acknowledged delivery systems like lipid nanoparticles, lipofectamine etc., for comparative understanding of their delivery system’s efficacy. If not, authors must at-least include these experiments in limitations and future directions/studies section as part of the conclusion.
  2. Include statistical analysis for data presented in figures 2, 3 and 4.

Author Response

please see the attachment

Author Response File: Author Response.docx

Back to TopTop