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- W4292303790 abstract "Since the second generation of controlled drug delivery evolution, nanocarriers have emerged as a promising platform for drug delivery. Many products in various areas such as cosmetics, industry, and agriculture have been developed based on this technology and delivered to the community to facilitate their usage and ensure maximum benefit. Moreover, many micelle formulations are either in clinical trial or approved for clinical application. Nevertheless, applications of this field in health have been limited by many challenges, the most important of which is the lack of unified standards for regulation and consistent methods for testing safety and quality. This underscores the need to explore new guidelines and regulations for nanocarriers. In this chapter, we will focus on the status of nanomicelle regulation together with the importance of regulation and current regulatory pathways. Furthermore, challenges facing regulation, nanomedicines’ status in the market, and clinical status of polymeric micelles will also be discussed." @default.
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- W4292303790 date "2022-01-01" @default.
- W4292303790 modified "2023-09-29" @default.
- W4292303790 title "Regulatory pathways and prospects for polymeric micelles" @default.
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- W4292303790 doi "https://doi.org/10.1016/b978-0-323-89868-3.00010-0" @default.
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