CRISPR systems should accumulate at disease sites and successfully penetrate nuclei. New characteristics are being studied to mediate cell selectivity, such as biophysical and topographic signals. Nanocarriers' long-term safety must be examined, as nanomaterial accumulation in the liver is detected with delayed removal. More basic scientific inquiry on nanotechnology-related toxicity and long-term animal monitoring is needed. Because urine excretion may eliminate degraded particles smaller than 5 nm, creating biodegradable nanocarriers can reduce long-term toxicity. Research on biomarker-regulated nanocarriers is limited, publishing only protease or ATP-responsive research. Using a stiff chain as a connection between target groups and nano-c carriers and polymers of suitable length, including targetable groups and negative charges to limit protein absorption, may assist. There are still gaps between research and clinical translation, we argue. We conclude that the utilization of direct usage of materials created by live beings is also an interesting way to imitate intrinsic cell identification and translocation capabilities. We believe that the development of CRISPR delivery nano carriers will be a novel tool for treating human illnesses with enormous translational potential.The Activatable probe design, which shifts to active conditions in the presence of biomarkers, can be utilized as a model. The circulatory half-life of most reported CRISPR nanocarriers is unknown, and a critical pharmacokinetic parameter remains unknown.Figuring out how to create large-scale nanocarriers while adhering to suitable manufacturing methods is vital and tough. The effects of scale-up on nanoparticles should be further investigated.