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There are, however, technical problems, including the poor penetration of light into deep tissues.
These drivers may have disadvantages in certain applications, such as poor penetration depth and inflexible orientation.
Most current imaging modalities either suffer from poor penetration depth or require exogenous contrast agents.
Technologies such as fluorescent proteins and optogenetics serve this purpose in small, translucent specimens, but are limited by the poor penetration of light into deeper tissues.
Poor penetration and excessive absorption of high frequencies limit spectroscopic approaches using fast rise pulses for inspecting many engineered structures.
One problem for many NPs is poor penetration into tumors, and thus the photokilling is not complete.
These problems include termite attack, disintegration due to flood water, mold buildups and poor penetration resistance against wind borne debris.
Various factors are responsible for the poor penetration of topical and systemic antibiotics in the vitreous.
Optical coherence tomography offered unexpectedly poor penetration due to the high optical attenuation coefficient of papyrus.
The cell performances are limited by the poor penetration of polymers into the porous nanocrystalline TiO2 network.
Several factors have been proposed to explain the poor penetration and distribution of GNPs in solid tumors.
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