Abstract

The necessity to develop more efficient, biocompatible, patient compliance, and safer treatments in biomedical settings is receiving special attention using nanotechnology as a potential platform to design new drug delivery systems (DDS). Despite the broad range of nanocarrier systems in drug delivery, lack of biocompatibility, poor penetration, low entrapment efficiency, and toxicity are significant challenges that remain to address. Such practices are even more demanding when bioactive agents are intended to be loaded on a nanocarrier system, especially for topical treatment purposes. For the aforesaid reasons, the search for more efficient nano-vesicular systems, such as nanoliposomes, with a high biocompatibility index and controlled releases has increased considerably in the past few decades. Owing to the stratum corneum layer barrier of the skin, the in-practice conventional/conformist drug delivery methods are inefficient, and the effect of the administered therapeutic cues is limited. The current advancement at the nanoscale has transformed the drug delivery sector. Nanoliposomes, as robust nanocarriers, are becoming popular for biomedical applications because of safety, patient compliance, and quick action. Herein, we reviewed state-of-the-art nanoliposomes as a smart and sophisticated drug delivery approach. Following a brief introduction, the drug delivery mechanism of nanoliposomes is discussed with suitable examples for the treatment of numerous diseases with a brief emphasis on fungal infections. The latter half of the work is focused on the applied perspective and clinical translation of nanoliposomes. Furthermore, a detailed overview of clinical applications and future perspectives has been included in this review.

Highlights

  • PROBLEM STATEMENT AND OPPORTUNITIESConventional drug delivery systems (DDS) are used to deliver therapeutic molecules into the human body either by oral consumption, injection, or topical administration

  • There is a dire need for highly effective and less/non-toxic alternatives to treat existing and emerging diseases. This has provoked the medical sector authorities to search for robust therapeutic agents and new ways to increase the efficacy of traditional drug delivery agents (Taboada and Grooters, 2008)

  • The present review focuses on the recent development in nanoliposome-based DDS with a brief emphasis on fungal infections

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Summary

Introduction

PROBLEM STATEMENT AND OPPORTUNITIESConventional drug delivery systems (DDS) are used to deliver therapeutic molecules into the human body either by oral consumption, injection, or topical administration. Scientists have engineered several types of nanocarrier mechanisms, such as solid lipid nanoparticles (SLN), liposomes, polymeric micelles, metallic nanoparticles (MNPs), spanlastics, nanoemulsions, nanoliposomes, among others (Taboada and Grooters, 2008; Elsherif et al, 2017; Huang et al, 2017; Zamani et al, 2018; Permana et al, 2019; Yang et al, 2020), either to develop new drug formulations or improve the existing ones Many of these nano-systems are capable of inducing/imparting pharmacological activities, enhance drug dynamism, and improve physical stability to attain controlled release characteristics (Haury et al, 2017). The newer nanomedicines with a topical approach can counteract the issues associated with conventional and systemic therapy for the treatment of infections and, at the same time, reducing the highcost impact and minimizing long-term side effects (Gupta et al, 2017)

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