2018
DOI: 10.1039/c8cc05552a
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Pro-guest and acyclic cucurbit[n]uril conjugated polymers for the controlled release of anti-tumor drugs

Abstract: We report "pro-guest" and acyclic cucurbit[n]uril conjugated polymers as supramolecular drug delivery systems (DDSs). These supramolecular DDSs could encapsulate anti-tumor drugs. Under acidic conditions, an acid-labile "pro-guest" degraded to become a "competing guest", which displaced and released the encapsulated drug at a tunable rate.

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Cited by 29 publications
(13 citation statements)
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“…Controlled drug release was not detected at pH 7.4. The drug‐loaded citraconic amide polymer displayed efficient internalization by HeLa cells at pH 6.0, attributed to the fast degradation [43] . Supramolecular assemblies combining CB[7], CB[8], and proteins have been explored for cancer photodynamic therapy by using various photosensitizers (acridine orange, methylene blue or cationic porphyrin).…”
Section: Macrocyclesmentioning
confidence: 99%
“…Controlled drug release was not detected at pH 7.4. The drug‐loaded citraconic amide polymer displayed efficient internalization by HeLa cells at pH 6.0, attributed to the fast degradation [43] . Supramolecular assemblies combining CB[7], CB[8], and proteins have been explored for cancer photodynamic therapy by using various photosensitizers (acridine orange, methylene blue or cationic porphyrin).…”
Section: Macrocyclesmentioning
confidence: 99%
“…Supramolecular chemotherapy is of great interest owing to the dynamic nature of noncovalent interactions that contributes to the protection of drugs and controlled release at target tissues. Among noncovalent interactions, host–guest interactions have been widely used to carry drugs that benefited from their tunable binding ability and a well-defined host–guest structure with an accurate binding ratio. ,, For supramolecular chemotherapy systems based on host–guest interactions, the strong binding affinity of the host to drugs is essential for efficient protection of drugs from a harsh physiological environment. However, a drug encapsulated in a stable binary host–guest complex is hard to be released by competitive guests, especially considering the low concentrations of competitive guests at target tissues. To date, some important advances have taken place to achieve controlled release of stably encapsulated drugs, ,, but it still remains a challenge to construct a supramolecular chemotherapy system equipped with both sufficient protection and highly effective release of drugs simultaneously.…”
Section: Introductionmentioning
confidence: 99%
“…And this supramolecular assembly is used for bioimaging in vitro with good biocompatibility . By modifying acyclic cucurbit[n]uril conjugated polymers with pro‐guest, pH‐responsive controlled release was achieved with a tunable rate based on ‘‘pro‐guest’’‐to‐guest conversion and cargo displacement …”
Section: Introductionmentioning
confidence: 99%